The Goodwill Store, 475 Hurffville - Cross Keys Rd, SEWELL, NJ, 08080, USA
Latest report:
Covid-19 OSHA Complaint
2 years ago
1. Employees are exposed but not limited to, rats and mice in the storage containers. 2. Employees are exposed to unsansitized working conditions and are not being provided appropriated agents during the COVID 19 pandemic. 3. Employees are being exposed to respiratory hazards where there is potential
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mold and an excessive black dust.
Alleged Hazards: 2, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-04-21
Alleged Hazards: 2, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2021-04-21
286
Related Reports
Snakes and feeder rodents linked to Salmonella Outbreak in Canada, Canada
3 weeks ago •source www.canada.ca
Outbreak
The Public Health Agency of Canada (PHAC) is investigating a Salmonella outbreak linked to snakes and feeder rodents across eight provinces. The outbreak has resulted in 70 confirmed cases of illness, 10 individuals have been hospitalized, and one fatality reported. The provinces affected include British Columbia (3),
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Alberta (10), Saskatchewan (7), Manitoba (3), Ontario (32), Quebec (11), New Brunswick (1) and Newfoundland and Labrador (3).
Many of the individuals who fell ill reported direct or indirect contact with snakes and feeder rodents before their illnesses occurred. Some did not handle the animals themselves but lived in the same house where they were kept. A single common supplier of snakes or feeder rodents has not been identified, indicating that Salmonella bacteria can be found in many species of animals, including snakes and feeder rodents.
The outbreak, which spans from British Columbia to Newfoundland and Labrador, has been ongoing since February 2022. The infected individuals range in age from 0 to 96, with 19% of the cases involving children 5 years or younger.
The issue was first identified due to an increase in reports of Salmonella illnesses across Canada. Through the use of whole genome sequencing, it was determined that some illnesses dating back to 2022 were caused by the same outbreak strain as the illnesses that occurred in 2023 and 2024. The investigation is ongoing, and recent illnesses continue to be reported to PHAC.
You can get sick with Salmonella by touching reptiles and rodents, their food, and their environments and then touching your face, eyes, or mouth without washing your hands. To prevent further spread of the disease, individuals are advised to practice good hand hygiene and frequent handwashing after contact with snakes, feeder rodents, and their environments.
In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: www.canada.ca/en/public-health/services/public-health-notices/2023/outbreak-salmonella-infections-linked-snakes-rodents.html
Many of the individuals who fell ill reported direct or indirect contact with snakes and feeder rodents before their illnesses occurred. Some did not handle the animals themselves but lived in the same house where they were kept. A single common supplier of snakes or feeder rodents has not been identified, indicating that Salmonella bacteria can be found in many species of animals, including snakes and feeder rodents.
The outbreak, which spans from British Columbia to Newfoundland and Labrador, has been ongoing since February 2022. The infected individuals range in age from 0 to 96, with 19% of the cases involving children 5 years or younger.
The issue was first identified due to an increase in reports of Salmonella illnesses across Canada. Through the use of whole genome sequencing, it was determined that some illnesses dating back to 2022 were caused by the same outbreak strain as the illnesses that occurred in 2023 and 2024. The investigation is ongoing, and recent illnesses continue to be reported to PHAC.
You can get sick with Salmonella by touching reptiles and rodents, their food, and their environments and then touching your face, eyes, or mouth without washing your hands. To prevent further spread of the disease, individuals are advised to practice good hand hygiene and frequent handwashing after contact with snakes, feeder rodents, and their environments.
In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Source: www.canada.ca/en/public-health/services/public-health-notices/2023/outbreak-salmonella-infections-linked-snakes-rodents.html
84
Unordered Package, Rancho Cucamonga, CA, USA
2 months ago •reported by user-rcgnq971
I received a package today that I DID NOT order from. a Jerry Yasfbara 9208 Charles Smith Ave. Rancho Cucamonga, California.
It was a tacky cheaply made sweatshirt with mice and a t shirt with paw prints.
It was a tacky cheaply made sweatshirt with mice and a t shirt with paw prints.
244
W
user-wwpy6342
Also received random package? Weird! Can't figure this scam out yet...
- 2 months ago
- Reply
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user-wwpy6342
I also received packages never order from Jerry Yasfbara, really weird
- 2 months ago
- Reply
G
user-ghtt8675
I JUST RECEIVED A PACKAGE JUST NOW FROM JERRY, I DID NOT ORDER NOTHING
- 2 months ago
- Reply
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user-wwpy6342
I received two rolls of postage stamps I didnt order. hmmmm..
- 2 months ago
- Reply
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user-wwpy6342
I received one roll of stamps today that I didn't order. Jerry must like you more.
- 2 months ago
- Reply
K
user-kqmcj485
anonymous 41534
I received Eye Massager and ear pods I did not order these!
- 2 months ago
- Reply
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user-wwpy6342
Received a Swarovski necklace with a receipt for $980. My accounts do not seem compromised. What do I do with this? Return to sender??
- 1 month ago
- Reply
R
user-rkbpq344
I receiv ed an open bag with nothing in it from the same Jerry. When I look up the address it is an office building. There are multiple mailing labels under the original and the package is open. I am going to investigate further.
- 1 month ago
- Reply
B
user-bbjcf692
I just received a Swarovski necklace from this person and address… anyone know what this might be about yet?
- 1 month ago
- Reply
Y
user-yjvzz155
I just received ear plugs that I never ordered…has anyone figured out this scam yet? Don’t see any unidentified charges on my account yet…
- 1 month ago
- Reply
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user-ypxfd334
I got a outfit with my daughters name on it… I haven’t ordered anything..
- 1 month ago
- Reply
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user-frbkd568
My parents have received 2 rolls of stamps twice from this guy. I think I will take to post office to see if legit.
- 1 month ago
- Reply
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user-pkkm8625
I ordered some Trump shoes, not sure who it was ordered from. It arrived but the shoes are about 2 sizes too big on me and no recourse to exchange them. I think the delivery was either post link or speedx. The tracking does not work on either. So in my case, I ordered these shoes but can’t remember from where and no email reply’s.
- 3 weeks ago
- Reply
Y
user-yzpmn436
My boyfriend received a blanket of his deceased mother who’s been gone almost ten years it’s weird and concerning that our information is breached
- 1 week ago
- Reply
Received items i did not order, 746 South Glasgow Avenue, Inglewood, CA, USA
3 months ago •reported by user-yyqb4441
Received business office wired mouse and a Smart Band 7
2.8K
Online Scam, Placentia, CA, USA
3 months ago •reported by user-mvny6234
I purchased two Black Falcon 7 Drones each costing $99, but I was shipped two $30.85 Drone Pro instead. I ordered 2 Black Falcon 4 drones from a web site that said they recommend the best Christmas gifts. I mouse clicked "Visit Site" and ended up placing
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the order at www.topdronecams.com/.
1.1K
Covid cases in my area are high, Rolla, MO, USA
4 months ago •reported by user-cvttz511
Covid number are spiking in the area, especially in the FedEx and UPS terminal, Missouri S&T and Rolla public school's.
92
T
user-tnvv1773
costco optical lab employees are using and selling drugs in the lab
- 1 month ago
- Reply
Power Outage, Washington Township, NJ, USA
2 months ago
According to JCP&L, about 1,759 customers were without power in Washington Township and 1,530 customers were without power in Parsippany as of 9:15 a.m. The power is expected to be restored by 11:30 a.m. There are also 1,669 customers affected in White and Oxford Townships.
Outage link: …
Outage link: …
outages.firstenergycorp.com/nj.html
Source: dailyvoice.com/new-jersey/morris/thousands-without-power-in-morris-county-towns/
Published: 2024-02-13
Source: dailyvoice.com/new-jersey/morris/thousands-without-power-in-morris-county-towns/
Published: 2024-02-13
286
According to the JCP&L's outage map, there are 3,974 customers affected in Hunterdon and Warren Counties.
Outage link: outages.firstenergycorp.com/nj.html
Source: newjersey.news12.com/power-outages-impact-multiple-new-jersey-towns
Published: 2023-09-08
Outage link: outages.firstenergycorp.com/nj.html
Source: newjersey.news12.com/power-outages-impact-multiple-new-jersey-towns
Published: 2023-09-08
66
Power Outage, Washington Township, NJ, USA
8 months ago •reported by user-zjyph488
Another power outage
286
Residents around Long Valley have reported outages Monday morning, according to Jersey Central Power & Light. Wires have fallen on the road near Bartley Road between Naughright and North 4 Bridges Roads, according to police, and motorists should seek alternate routes. According to the Washington Township Office
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of Emergency Management, more than 450 customers are currently without power in the area.
Outage link: outages.firstenergycorp.com/nj.html
Source: patch.com/new-jersey/longvalley/power-outages-downed-wires-long-valley-0
Published: 2023-06-26
Outage link: outages.firstenergycorp.com/nj.html
Source: patch.com/new-jersey/longvalley/power-outages-downed-wires-long-valley-0
Published: 2023-06-26
127
Power Outage, West Mill Road & Beacon Hill Road, Long Valley, Washington Township, NJ, USA
10 months ago
A tree and wires have fallen on the road near #518 West Mill Road and Beacon Hill Road, According to Jersey Central Power & Light (JCP&L), more than 100 customers are currently without power in the area.
Outage link: outages.firstenergycorp.com/nj.html
Source: patch.com/new-jersey/longvalley/power-outages-downed-wires-long-valley
Published: 2023-06-14
Outage link: outages.firstenergycorp.com/nj.html
Source: patch.com/new-jersey/longvalley/power-outages-downed-wires-long-valley
Published: 2023-06-14
27
Recent Interesting Reports
Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol, USA
1 week ago •source www.fda.gov
Recall notice
Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in
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the US online only via the Aruba Aloe Balm N.V. website. To date, Aruba Aloe Balm N.V. has not received any reports of adverse events related to these products.
Aruba Aloe Hand Sanitizer Gel is used as a sanitizer to help reduce bacteria that potentially can cause disease and is packaged in 12 fl oz (355 mL) dark green plastic bottles with white label reading in part “ARUBA ALOE Hand Sanitizer GEL 80% Alcohol Made in Aruba World’s Finest Aloe”, with barcode 0 82252 03300 5.
Aruba Aloe Alcoholada Gel is used for temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations and is packaged in two sizes: 2.2 fl oz (65 mL) plastic bottles with barcode 0 82252 34030 1 and 8.5 fl oz (251 mL) plastic bottles with barcode 0 82252 03120 9. The plastic bottles are transparent with a label reading in part “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride”.
The affected Aruba Aloe Hand Sanitizer GEL product lots (filled in 12, 2.2, and 8.5 fl. oz bottles bottles) can be viewed in the link below.
Aruba Aloe Balm N.V. has notified all customers that bought these products by email and has offered a discount coupon for a next purchase. Consumers that have products which are being recalled should stop using and discard the product.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Aruba Aloe Balm N.V.
Brand name: Aruba Aloe
Product recalled: Hand Sanitizer Gel and Alcoholada Gel
Reason of the recall: Product contains methanol
FDA Recall date: April 05, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aruba-aloe-balm-nv-issues-voluntary-nationwide-recall-aruba-aloe-hand-sanitizer-gel-alcohol-80-and
Aruba Aloe Hand Sanitizer Gel is used as a sanitizer to help reduce bacteria that potentially can cause disease and is packaged in 12 fl oz (355 mL) dark green plastic bottles with white label reading in part “ARUBA ALOE Hand Sanitizer GEL 80% Alcohol Made in Aruba World’s Finest Aloe”, with barcode 0 82252 03300 5.
Aruba Aloe Alcoholada Gel is used for temporary relief of pain and itching associated with minor burns, sunburn, insect bites, or minor skin irritations and is packaged in two sizes: 2.2 fl oz (65 mL) plastic bottles with barcode 0 82252 34030 1 and 8.5 fl oz (251 mL) plastic bottles with barcode 0 82252 03120 9. The plastic bottles are transparent with a label reading in part “Alcoholada Gel Pain Relieving Gel 0.5% Lidocaine Hydrochloride”.
The affected Aruba Aloe Hand Sanitizer GEL product lots (filled in 12, 2.2, and 8.5 fl. oz bottles bottles) can be viewed in the link below.
Aruba Aloe Balm N.V. has notified all customers that bought these products by email and has offered a discount coupon for a next purchase. Consumers that have products which are being recalled should stop using and discard the product.
Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache blurred vision, coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Aruba Aloe Balm N.V.
Brand name: Aruba Aloe
Product recalled: Hand Sanitizer Gel and Alcoholada Gel
Reason of the recall: Product contains methanol
FDA Recall date: April 05, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/aruba-aloe-balm-nv-issues-voluntary-nationwide-recall-aruba-aloe-hand-sanitizer-gel-alcohol-80-and
303
Scam, NYC, NY, USA
1 week ago •reported by user-kggw2784
Is your facility a distributor for an overseas market? I received a bracelet I didn’t order and didn’t get 2 bag charms I did order from HGate. Already opened a dispute with them .
2.8K
Same thing, Dallas, TX, USA
4 days ago •reported by user-vcjnp739
I placed a order on March 12th from the same company and got a tracking number stayed watching it as it supposedly went to each destination till it stated delivered on March 27th. But nothing came, my husband stayed my the front door all day waiting for
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it, for nothing to arrive. I've reached out to customer service with no success to do anything. And im out of $150 of my hard working money just gone...... I'm so upset don't know who to turn to. The website stated they were affiliated with Amazon and it was a secured site so I believed it was ok...... how can they use a logo of such magnitude and not be real???
786
Not ordered products, Tampa, FL 33675, USA
4 weeks ago •reported by user-bknwr732
I got this shit in the mail and through local law enforcement officials investigating a fraudulent transaction case, you were determined to be the thief. Where do you want this shit sent from here you thief?
This package arrived addressed to me, I opened it and found …
This package arrived addressed to me, I opened it and found …
the product inside that I never ordered. I don’t want it and refuse to pay for something I didn’t order. What should I do with it?
USPS tracking number 9400111206217603******. There has been a investigation started by the the one police Department and fraud charges are being charged against your company for stealing money for my social security pay for this product.
Im in Des Moines, IA, USA
USPS tracking number 9400111206217603******. There has been a investigation started by the the one police Department and fraud charges are being charged against your company for stealing money for my social security pay for this product.
Im in Des Moines, IA, USA
523
Scam, Michigan, USA
1 week ago •reported by user-rrfzf831
I never ordered anything and they keep sending me shit!
198
Alert of a cluster of Illnesses resembling Botulism from possibly Counterfeit Botox, LaSalle County, IL, USA
6 days ago •source dph.illinois.gov
Outbreak
The Illinois Department of Public Health (IDPH) has issued an alert regarding a potential botulism outbreak linked to possibly counterfeit Botox injections. The alert follows the hospitalization of two individuals in LaSalle County who exhibited symptoms similar to botulism after receiving the injections. The issue came to
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light after the patients presented with symptoms resembling botulism. The IDPH, in collaboration with the LaSalle County Health Department and the Illinois Department of Professional Regulation (IDFPR), is currently investigating the matter. A similar cluster of cases was also reported by the Tennessee Department of Health, prompting the IDPH to liaise with the CDC and FDA for further investigation.
The product in question is either Botox or a possibly counterfeit version of the product, and it was administered by a licensed nurse in LaSalle County who was performing work outside her authority. The two affected individuals reported symptoms such as blurred/double vision, droopy face, fatigue, shortness of breath, difficulty breathing, and hoarse voice following the injection. Both required hospitalization post-treatment.
People are advised not to use these botox injections. In Illinois, the injection of botulinum toxin, the key ingredient in Botox, is a practice of medicine that may only be performed by certain licensed professionals who are licensed and regulated by IDFPR. Cosmetologists and estheticians are prohibited from performing this practice under their licenses.
Botulism is a serious illness caused by a toxin produced by the Clostridium botulinum bacteria. This toxin is one of the most potent neurotoxins known and can cause muscle paralysis. The disease can manifest in three forms: foodborne botulism, wound botulism, and infant botulism. Foodborne botulism, which is the focus here, occurs when food contaminated with the bacteria is consumed. Symptoms can include difficulty swallowing or speaking, facial weakness, and paralysis. In severe cases, it can be fatal, particularly if it affects the respiratory muscles.
If you or a loved one are harmed or experiencing any symptoms, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.
Source: dph.illinois.gov/resource-center/news/2024/april/2024-04-08---idph-alerts-healthcare-providers-to-cluster-of-illn.html
The product in question is either Botox or a possibly counterfeit version of the product, and it was administered by a licensed nurse in LaSalle County who was performing work outside her authority. The two affected individuals reported symptoms such as blurred/double vision, droopy face, fatigue, shortness of breath, difficulty breathing, and hoarse voice following the injection. Both required hospitalization post-treatment.
People are advised not to use these botox injections. In Illinois, the injection of botulinum toxin, the key ingredient in Botox, is a practice of medicine that may only be performed by certain licensed professionals who are licensed and regulated by IDFPR. Cosmetologists and estheticians are prohibited from performing this practice under their licenses.
Botulism is a serious illness caused by a toxin produced by the Clostridium botulinum bacteria. This toxin is one of the most potent neurotoxins known and can cause muscle paralysis. The disease can manifest in three forms: foodborne botulism, wound botulism, and infant botulism. Foodborne botulism, which is the focus here, occurs when food contaminated with the bacteria is consumed. Symptoms can include difficulty swallowing or speaking, facial weakness, and paralysis. In severe cases, it can be fatal, particularly if it affects the respiratory muscles.
If you or a loved one are harmed or experiencing any symptoms, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.
Source: dph.illinois.gov/resource-center/news/2024/april/2024-04-08---idph-alerts-healthcare-providers-to-cluster-of-illn.html
27
I ordered off Zedong Information Technology on 6th April a pair of sandals at £22.98 that was including p and p. I have since received no communication or sandals. I have also realised that the site or company are scammers and do not send genuine customer
72
I received a jar of subjenix bioribose that I did not order., San Francisco, CA, USA
1 day ago •reported by user-qpqwb441
I received a package of this in the mail. I did not order it. Nothing else came with it no papers or anything I will dispose of it. They have my address in my full name and I am not sure how this company got it.
633
Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
1 week ago •source www.fda.gov
Recall notice
Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good
…
manufacturing practice (cGMP) requirements. To date, Honeywell Safety Products USA, Inc. has not received any reports of adverse events related to this recall.
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
303
Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super poteny risk, USA
2 weeks ago •source www.fda.gov
Recall notice
Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL, 150 mL, or 300 mL pack sizes, to the Consumer Level. Some bottles may have been overfilled which can
…
result in an over-potent dosing regimen. The affected Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL lots were distributed Nationwide in the USA directly to Wholesalers and Distributors. The Lots were distributed between 11/09/2023 and 2/20/2024. To date, Amneal has not received any reports of adverse events that have been confirmed to be directly related to this recall.
Risk Statement: Adult patients who are prescribed the maximum daily dose of up to 2 grams per day of Vancomycin Hydrochloride for oral solution, USP 250 mg/5mL, may receive up to 4 grams of oral vancomycin per day because of the overfilled bottle. Some patients with inflammatory disorders of the intestinal mucosa also may have significant systemic absorption of vancomycin. These patients may be at risk for the development of adverse reactions associated with higher doses of vancomycin oral solution. Worsening renal function could be associated with electrolyte abnormalities such as high potassium leading to cardiac arrest.
The recommended maximum daily dose allowance for this product is up to 2gm/day and patients prescribed a dosing regimen of 500 mg/10mL would exceed this daily allowance, which may be harmful to patients with renal insufficiency. The error occurred during the manual bottle filling stage of manufacturing.
Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL, is administered orally for treatment of enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains) and antibiotic- associated pseudomembranous colitis caused by C. difficile.
The Vancomycin HCl for Oral Solution, USP, 250 mg/5mL subject to the recall, are identified by the NDC numbers stated on the product label. The following lot numbers of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL are included in this recall.
Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL.
- Pack Size: 80 mL, Expiration Date: 09/2025, Lot: 22613003A, NDC No.: 69238-2261-3.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613004A, NDC No.: 69238-2261-7.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613005A, NDC No.: 69238-2261-7.
- Pack Size: 300 mL, Expiration Date: 09/2025, Lot: 22613005B, NDC No.: 69238-2261-5.
Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Retailers who have Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL, which are being recalled, should examine their inventory and cease dispensing any of the impacted lots.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Amneal Pharmaceuticals, LLC.
Brand name: Amneal
Product recalled: Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL
Reason of the recall: Super potent due to bottles being overfilled
FDA Recall date: March 27, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-nationwide-voluntary-recall-vancomycin-hydrochloride-oral-solution
Risk Statement: Adult patients who are prescribed the maximum daily dose of up to 2 grams per day of Vancomycin Hydrochloride for oral solution, USP 250 mg/5mL, may receive up to 4 grams of oral vancomycin per day because of the overfilled bottle. Some patients with inflammatory disorders of the intestinal mucosa also may have significant systemic absorption of vancomycin. These patients may be at risk for the development of adverse reactions associated with higher doses of vancomycin oral solution. Worsening renal function could be associated with electrolyte abnormalities such as high potassium leading to cardiac arrest.
The recommended maximum daily dose allowance for this product is up to 2gm/day and patients prescribed a dosing regimen of 500 mg/10mL would exceed this daily allowance, which may be harmful to patients with renal insufficiency. The error occurred during the manual bottle filling stage of manufacturing.
Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL, is administered orally for treatment of enterocolitis caused by Staphylococcus aureus (including methicillin-resistant strains) and antibiotic- associated pseudomembranous colitis caused by C. difficile.
The Vancomycin HCl for Oral Solution, USP, 250 mg/5mL subject to the recall, are identified by the NDC numbers stated on the product label. The following lot numbers of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL are included in this recall.
Vancomycin Hydrochloride for Oral Solution, USP, 250mg/5mL.
- Pack Size: 80 mL, Expiration Date: 09/2025, Lot: 22613003A, NDC No.: 69238-2261-3.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613004A, NDC No.: 69238-2261-7.
- Pack Size: 150 mL, Expiration Date: 09/2025, Lot: 22613005A, NDC No.: 69238-2261-7.
- Pack Size: 300 mL, Expiration Date: 09/2025, Lot: 22613005B, NDC No.: 69238-2261-5.
Anyone with an existing inventory of the product being recalled should examine the product and quarantine any of the recalled lots immediately. Retailers who have Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL, which are being recalled, should examine their inventory and cease dispensing any of the impacted lots.
In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.
Company name: Amneal Pharmaceuticals, LLC.
Brand name: Amneal
Product recalled: Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL
Reason of the recall: Super potent due to bottles being overfilled
FDA Recall date: March 27, 2024
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/amneal-pharmaceuticals-llc-issues-nationwide-voluntary-recall-vancomycin-hydrochloride-oral-solution
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