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Report a health, safety, or community issue here! Like, follow and comment. Help keep friends family and community safe and aware. Trending topics on SafelyHQ:   #DeliveryIssue #OnlineScam #EmptyPackageScam #PowerOutages  #BoilWaterAdvisory #OccupationalHealth&Safety

#Empty Package

9 hours ago

Received a package with a small cardboard. I live in California. Seems like other people have gotten the same thing happened to them. How do I contact the company and is the is dangerous? No idea who sent it

#emptypackage #delivery #1007brynmawrdrive #papillion #nebraska #unitedstates See Less
1


#Pet Food

5 days ago

My dog is so sick from these dreambone triple flavor twisties. I had to rush him to vet. He has bloody diarrhea and throwing up all night. Just buy some vegetables or chicken and cook for a treat, cheaper than this crap from China | Symptoms: Vomiting, Bloody Stool See Less
346


#Power Outages

3 hours ago

CPS Energy is reporting a power outage in Leon Valley that has left more than 3,800 customers without power early Monday morning. The energy company said they became aware of the outage around 4:25 a.m. Updated at 5:55 a.m.: The outage has been resolved, according to CPS... See More Energy’s online outage map.

Outage link: outagemap.cpsenergy.com
Source: ksat.com
Published: 2022-12-05
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#Reckless Driving

3 weeks ago

A hit and run accident this morning involving an Amazon driver.  I don’t know how to reach the Amazon warehouse on Old Statesville Road in Charlotte.  I cannot find their phone number.  The accident occurred at the intersection of WT Harris Boulevard and Lakeview Road. At that... See More traffic light. It was at 6:25 am. See Less
1.4K


#Boil Water Advisory

3 hours ago

Some residents of Marion County are under a precautionary water boil notice. Marion County Utility Officials issued this notice for people who live in Hunters Trace and Pine Ridge Estates after a temporary drop in water pressure. Customers in these communities should use bottled water or bring... See More water to a rapid boil for 1 minute before using it to drink, cook or brush their teeth.

Source: wcjb.com
Published: 2022-12-05
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#Amazon

5 days ago

I did order an item on Amazon returns sale. But not this item. I ordered on amazon pallet sale, I specified electronics. So I was very surprised to receive a fountain pen, which sells for quite a bit less than what they are selling this Dolin foutian... See More pen . Not to happy at all, I guess you really can’t trust when you are purchasing from without really researching it. But since it was associated with Amazon I did not think it would be a scam. See Less
723


EL
e..............0
Lol how does have anything to with anything like a virus
Reply 4 days ago
There is not enough bathrooms for the amount of workers on site. Job has picked up and the number of workers has increased but additional bathrooms have not been added to accommodate. In turn this is causing disgusting conditions before scheduled cleaning. Brought it up to Holland... See More but unfortunately was ignored and my concerns were treated in their opinion inadequate. I shouldn’t have to use a disgusting restroom. See Less
1.6K


#Drugs

3 days ago

Medicine for OAB Trospium Chloride 20mg - first 3 pills worked fine 4th pill not the same was like a strong diet pill kept me up all night with heart beating too fast the following days heart was still beating faster than normal - I reported the... See More problem to the pharmacy and my Doctor and discontinued the pill. It was unstable medicine did not make any sense - I was going to the bathrrom too many times at night for a long period of time | Symptoms: Diarrhea, Other See Less
1.6K


#Medical Devices

1 year ago

I purchased the metre from boots chemist about 5 months ago and have just realised it measures in mmol/L I see there is a recall out on this metre, what should I do 💁‍♀️ See Less
429


#COVID-19

1 month ago

As a bus driver I was precautionary about wearing a safety mask while riding the bus. Later I found that when I took my mask off at work I caught COVID 19 See Less
2.7K


#False Advertising

1 month ago

I ordered as advertised a Unbreakable Wire Trimmer Blade for $26.98 with shipping, ins and tax total about $42. Received confirmation and tracking number. Few days later got another tracking number with a derusting weeding wheel item inside show a label from usps from Online Seller 188... See More S Mountain House Parkway Tracy. This is not what I wanted tried calling get busy signal. I'm in Stockton, CA, USA See Less
3.2K


R0
anonymous7240
How was your issue resolved? I got 2 exact same packages of data cable sets. Scam of some kind.
Reply 1 month ago
BB
b........2
It never was resolved. got ripped-off instead! Stay away from this company!!!!!
Reply 1 month ago
DP
d......h
I got a package today with a scarf I did not order. Don't think I was charged for it. Anybody get charged for these packages???
Reply 2 weeks ago
YV
anonymous8049
I got an ugly pair of men's gloves today I didn't order from "online seller"
Reply 1 week ago
A supplement called captain boss bully ruby 10000 made my eyes burn,water,skin burn, vomiting, shaking, goosebumps. One of the worst experiences of my life

I bought it at a convenience store witch was prob my first mistake. I’ve taken them before and never had any issues. It... See More was the only brand left so I have it a go 20 minutes later my fave and eyes started burning and my eyes got really red. I got home around 830 took a shower and no longer then 5 min started puking none stop. It’s been going on for 3 hrs. Dizzy, goosebumps and worst of all I’m not in the mood whatsoever now. | Symptoms: Vomiting, Shaking See Less
525


Aqua Water said the boil water notice that was issued for Elgin residents on Blisard Road Friday has been lifted. Residents can resume using the water without any special treatment.

Source: cbsaustin.com
Published: 2022-12-04 See Less
58


#UPS

2 weeks ago

I received an item I did not order. Return address states Online Seller, 2646 Rainier Ave S, Seattle, WA 98144. Underneath the UPS label it shows from China Post. I live in Indiana See Less
1.6K


NW
anonymous7984
Me too have any information on it?
Reply 1 week ago
SA
Safelyhq Support
Hi, thanks for your comment. We are investigating your cases and others like it, we are trying to understand more, and raise awareness, to help get this stopped. We recently got some coverage about people receiving packages that they didn't order, you can read more here: https://nypost.com/2022/10/12/empty-envelopes-in-the-mail-blamed-on-amazon-sellers/
Reply 5 days ago
Nestlé Purina PetCare Company is voluntarily recalling a limited amount of Purina Pro Plan Veterinary Diets EN Gastroenteric Low Fat (PPVD EN Low Fat) prescription wet dog food in 13.4 oz cans due to a labeling error. For a brief period on September 15, 2022, cans of... See More a different complete and balanced adult dog food, Purina ONE True Instinct Tender Cuts In Gravy With Real Turkey & Venison wet dog food, were labeled as PPVD EN Low Fat in one of our factories. The mislabeled diet is safe to feed, but it is not the intended formula for dogs requiring a prescription PPVD EN Low Fat diet, who may have sensitivities to traditional diets or difficulty digesting fat. While we have not received any reports to date of illness or injury to dogs fed this mislabeled product. The affected product was available by prescription only and distributed through veterinary clinics and other retailers with the ability to validate a prescription.

You can identify the mislabeled product by the UPC (38100 17599), production code (22581159 L4TR6) and “Best Before Sept 2024” date on the bottom of each PPVD EN Low Fat can.

We became aware of the issue after being contacted by several pet owners who observed the texture of food in their PPVD EN Low Fat cans was not the same as previous meals. The mislabeled product contains chunks in gravy, while the correct product looks more like a pate consistency.

We are conducting this voluntary recall as a precaution. We have asked our veterinary and other retail partners to remove the affected product. We also recommend that you discard any of the affected product you may have, and we will replace it as quickly as possible.

No other Purina products are impacted by this voluntary recall. We apologize to pet owners for any concerns or inconvenience this situation has caused. We’re pet owners too, and we know how important the health and well-being of our pets is, which is what led us to make this decision. We are taking action to investigate and notify pet owners and veterinarians of the situation. At Purina, pets always come first.

Company name: Nestle Purina PetCare Company
Product recalled: Purina Pro Plan Veterinary Diets EN Gastroenteric Low Fat (PPVD EN Low Fat) prescription wet dog food
Reason of the recall: Mislabeling / Labeling error
FDA Recall date: December 02, 2022

Source: fda.gov
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GlaxoSmithKline Consumer Healthcare ULC is recalling one lot of TUMS Peppermint Regular Strength tablets after some tablets were found to contain fragments of fibreglass and other material, including paper and aluminum foil. The product is sold in a package of three rolls containing 12 tablets each, and... See More was distributed across Canada starting on October 25, 2022.

The recalled product is:
- TUMS Peppermint Regular Strength (500mg) tablets, packages of three rolls of 12 tablets, NPN: 01970240, Lot: HA7H, Expiry: August 2027

Company name: GlaxoSmithKline Consumer Healthcare ULC
Product recalled: TUMS Peppermint Regular Strength (500mg) tablets, packages of three rolls of 12 tablets
Reason of the recall: Due to contamination fragments of fibreglass and other material
CFIA Recall date: November 30, 2022

TUMS is an antacid indicated for adult use to relieve indigestion and heartburn caused by too much acid in the stomach. If consumed, the fragments should pass through most people's digestive systems with no concern; however, elderly people and people who have narrow areas in their intestines because of disease or surgery may be at risk of injury.

Stop using the recalled product. Follow municipal or regional guidelines on how to dispose of chemicals and other hazardous waste; or Return the product to your local pharmacy for proper disposal.

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.

Source: recalls-rappels.canada.ca
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60


The Laundress New York issued a safety notice to stop using all their products due to the potential presence of elevated levels of bacteria in some of its products. These Bateria identified in product testing are so-called "opportunistic" pathogens, including Pseudomonas, which occur naturally in water and... See More soil. At the levels detected, these types of bacteria could present a risk of infection. To date, they are not aware of any adverse health impacts related to this issue.

You can see the list of the affected products here: thelaundresssafetynotice.com

The Laundress advises consumers to not use their products no matter if the product is or is not on the affected product list until their work with the US Consumer Product Safety Commission and Health Canada is complete. The investigation is ongoing.

People with a healthy immune system are usually not affected by these bacteria. People with weakened immune systems or external medical devices who are exposed to Pseudomonas face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin.

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.

Source: thelaundress.com
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472


DR
D.......s
Unable to pull up list of products from the link in your article
Reply 3 days ago
Rocky Mountain Pies, LLC of Salt Lake City, Utah is recalling 31.88 oz French Silk Pie with inkjet code date 2 266, because it may contain undeclared almonds. People who have an allergy or severe sensitivity to Tree Nuts (almonds) run the risk of serious or life-threatening... See More allergic reaction if they consume these products. Red Button Vintage Creamery French Silk Pie was distributed in Arizona, Utah, Oregon, Washington, Montana, Nevada, Colorado, Wyoming, and Idaho in retail stores. No illnesses have been reported to date.

Products are packaged in a clear plastic dome and black plastic base with a “Red Button Vintage Creamery” cardboard sleeve. Recall includes only products with the inkjet code on the dome that begins with “2 266”.  Only UPC code 0 41172 81290 9 is involved in this recall.

It was discovered at a retail location by staff that cases labeled “Turtle Cream Pies” contained Turtle Cream Pies, but were labeled with the “French Silk Pie” sleeves, resulting in the undeclared allergen, as the Turtle Cream Pie contains almonds and the French Silk Pie Sleeve does not declare almonds. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's pre-operational changeover packaging process. Consumers who have purchased Red Button Vintage Creamery French Silk Pie with the Lot Code beginning with “2 266” are urged to return it to the place of purchase for a full refund.

In case you experienced harm from allergens or undeclared ingredients, 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: Rocky Mountain Pies, LLC
Brand name: Red Button Vintage Creamery
Product recalled: French Silk Pie
Reason of the recall: Undeclared almond
FDA Recall date: November 29, 2022

Source: fda.gov
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63


Exela Pharma Sciences, LLC, (Exela) is expanding their recall, adding fourteen (14) lots to the ongoing voluntary recall of forty-nine (49) lots of Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL vial, 20-count carton. A total of 63 lots are now being recalled to the consumer level.... See More All the recalled lots are listed in the table below, with the additional fourteen (14) lots shown in BOLD and RED. The additional lots were distributed October 26, 2021 through April 25, 2022. Product was distributed nationwide to wholesalers, distributors, and other customers between October 26, 2021 and August 10, 2022. There have been no reports of sterility failures to date with any of the sixty-three (63) lots.

Risk Statement: The product poses a potential safety concern with vial breakage and flying glass when pressurized while preparing the product for administration. There is a potential of flying glass injuring skin, eye and/or other parts which could result in either temporary or permanent injury. Within the sixty-three (63) total recalled lots (which includes more than 2.7 million vials), Exela has received five (5) reports of flying glass injuring skin, eye and/or other parts. There have been no complaints of vial breakage or injuries related to the additional fourteen (14) lots.

Exela did not recall the additional fourteen (14) lots previously because they did not appear to be impacted. During the latest inspection of Exela’s retain product from the fourteen (14) lots, one (1) vial showed breakage. There have been no field reports of personal injury to date across all the sixty-three (63) lots since the recall process started. However, out of an abundance of caution, Exela is adding the 14 lots to the on-going recall. The product is used for treatment of metabolic acidosis and is packaged in a 50 mL glass vial, 20 vials per carton. The vials are labeled with Exela brand (Carton NDC: 51754-5001-5; Vial NDC: 51754-5001-1, Figure 1) and Civica brand (Carton NDC: 72572-740-20; Vial NDC: 72572-740-1, Figure 2). The affected Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL lots (covering both Exela and Civica brands) include the following lot numbers and expiration dates:

- Brand : Exela . Lot : P0001178 . Expire Date: 05/2023.
- Brand : Exela . Lot : P0001298 . Expire Date: 08/2023.
- Brand : Exela . Lot : P0001301 . Expire Date: 08/2023.
- Brand : Exela . Lot : P0001313 . Expire Date: 08/2023.
- Brand : Exela . Lot : P0001314 . Expire Date: 08/2023.
- Brand : Exela . Lot : P0001317 . Expire Date: 08/2023.
- Brand : Exela . Lot : P0001330 . Expire Date: 09/2023.
- Brand : Exela . Lot : P0001370 . Expire Date: 10/2023.
- Brand : Exela . Lot : P0001371 . Expire Date: 10/2023.
- Brand : Exela . Lot : P0001372 . Expire Date: 10/2023.
- Brand : Exela . Lot : P0001433 . Expire Date: 11/2023.
- Brand : Exela . Lot : P0001434 . Expire Date: 11/2023.
- Brand : Exela . Lot : P0001442 . Expire Date: 11/2023.
- Brand : Exela . Lot : P0001443 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001464 . Expire Date: 09/2023.
- Brand : Exela . Lot : P0001467 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001468 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001469 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001470 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001472 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001486 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001495 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001505 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001506 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001509 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001510 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001511 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001512 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001532 . Expire Date: 12/2023.
- Brand : Exela . Lot : P0001560 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001561 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001562 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001564 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001566 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001567 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001568 . Expire Date: 01/2024.
- Brand : Exela . Lot : P0001571 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001572 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001573 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001574 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001578 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001579 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001580 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001583 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001586 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001587 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001588 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001593 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001594 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001610 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001618 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001619 . Expire Date: 02/2024.
- Brand : Exela . Lot : P0001644 . Expire Date: 03/2024.
- Brand : Exela . Lot : P0001645 . Expire Date: 03/2024.
- Brand : Exela . Lot : P0001646 . Expire Date: 03/2024.
- Brand : Exela . Lot : P0001654 . Expire Date: 02/2024.
- Brand : Civica . Lot : P0001490 . Expire Date: 12/2023.
- Brand : Civica . Lot : P0001497 . Expire Date: 12/2023.
- Brand : Civica . Lot : P0001600 . Expire Date: 02/2024.
- Brand : Civica . Lot : P0001663 . Expire Date: 03/2024.

The Exela product (Carton NDC: 51754-5001-5; Vial NDC: 51754-5001-1) can be identified by the NDC numbers, and by the yellow flip-top safety cap on the 50 mL vial. The carton bears a purple stripe containing concentration information and the manufacturer name “Exela Pharma Sciences” in the lower right-hand corner. The vial label bears a purple stripe containing concentration information with the name “Exela Pharma Sciences” on the back.

The Civica Product (Carton NDC: 72572-740-20; Vial NDC: 72572-740-1) can be identified by the NDC numbers, by the yellow flip-top safety cap on the 50 mL vial, and by the carton which bears a green stripe containing concentration information and the manufacturer name “Civica” in the lower right-hand corner. The vial label bears a green stripe containing concentration information with the name “Civica” on the back.

All the above-listed lots are supplied in 20 count cartons only. This recall is not expected to cause drug shortage.

Customers that have product which is being recalled should discontinue use, segregate the recalled product, submit a recall stock response form to Exela (even if there is no product to return).

In case you experienced 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.

Company name: Exela Pharma Sciences, LLC
Brand name: Exela
Product recalled: Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL vial
Reason of the recall: Vial Breakage
FDA Recall date: November 29, 2022

Source: fda.gov
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472


The Arizona Department of Health Services (ADHS) announced the recall of specific marijuana products cultivated by PP Wellness due to possible contamination with Aspergillus, a fungus that can cause allergic reactions or infection, usually in people already sick with something else. These products were sold at multiple... See More locations with the product names listed below. To date, no illnesses have been reported.

The recalled products are:
Cultivator / Product Name / Batch Number / Product Type / Implicated Contaminant
- PP Wellness / El Alquimista / GH401 / Plant, Trim / Aspergillus
- PP Wellness / Tangie Head /GH403 / Plant, Trim / Aspergillus
- PP Wellness / Nasty Girl /GH404 / Plant, Trim / Aspergillus
- PP Wellness / The Juice / GH408/ Plant, Trim / Aspergillus
- PP Wellness / Gorilla Grapevine / GH413/ Plant, Trim / Aspergillus
- PP Wellness / The Juice / GH416 / Plant, Trim / Aspergillus

This announcement is being made out of an abundance of caution. Patients who have purchased potentially contaminated products should not ingest, inhale, or otherwise consume them and should dispose of them. Once ADHS discovered the positive test results, the establishment involved took immediate action to work with all distribution and retail partners to remove any potentially impacted products.

Aspergillus can cause allergic reactions or infections, usually in people already sick with something else. Symptoms range from asthma or cold-like symptoms to fever and chest pain among many others.

In case you experience harm from products, 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.

Source: azdhs.gov
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65


Mason Vitamins Inc. has issued a nationwide voluntary recall of the specific lot of Healthy Sense Daily Multiple with Iron and People’s Choice Women's Daily Vitamins with Iron due to Vitamin A, Vitamin B12, Vitamin C, Vitamin E and Pantothenic Acid amounts being lower than the declared... See More amount on the label which was determined during an FDA inspection. The products were sold nationwide at Bargain Barn, 99 Cents Only, Fruth Pharmacy, Joe V’s Smart Shop, Rose’s Discount Stores, Rex Discount Pharmacy, Star Discount Pharmacy, Propst Discount Pharmacy, Dollar Tree and limited distributors. To date, no illnesses related to these products have been reported.

Product Name: Healthy Sense Daily Multiple with Iron, Size: 20 tablets, UPC Code: 311845353238, Lot/Expiration Date: 25807G / 09/2024
Product Name: People’s Choice Women’s Daily Vitamins with Iron, Size: 30 tablets, UPC Code: 311845486882, Lot/Expiration Date: 25807G / 09/2024; A25807G / 09/2024; B25807G / 09/2024;C25807G / 09/2024; D25807G / 09/2024

No other People’s Choice and Healthy Sense products are affected by this recall. If customers have product affected by this voluntary recall, they should discard it immediately.

In case you experienced harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Mason Vitamins Inc.
Brand name: Healthy Sense and People’s Choice
Product recalled: Daily multi vitamin with Iron and Women’s daily vitamin with iron
Reason of the recall: Due to Vitamin 1, B12, C, E and Pantothenic Acid being lower than declared
FDA Recall date: November 17, 2022

Source: fda.gov
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472


Insulet Corporation (NASDAQ: PODD) (Insulet or the Company), today announced a Medical Device Correction for the Omnipod® 5 Automated Insulin Delivery System because of an issue with the Omnipod 5 Controller charging port and cable. This does not impact the Omnipod 5 Pod, the Omnipod® DASH Insulin... See More Management System, the Omnipod® Insulin Management System, or compatible Android smartphone devices that have the Omnipod 5 App installed. These actions are taken voluntarily with the knowledge of the FDA. Insulet has received 24 reports that the Omnipod 5 Controller charging port (USB-C port) or cable (USB cable) are melting, deforming, or discoloring due to heat generated by a poor connection between the cable and the port.

The excess heat may cause minor burns if those areas of the Controller are touched or could lead to fire. No serious injuries have been reported to Insulet as a result of this issue.

Omnipod 5 users are being notified by email with instructions on how to detect and reduce the risk of an issue with the charging port or cable.

In case you experienced issues with this product, it is important to report it.

Company name: Insulet Corporation
Brand name: Insulet Corporation Omnipod
Product recalled: Automated Insulin Delivery System
Reason of the recall: Issue with the Omnipod 5 Controller charging port and cable
FDA Recall date: November 15, 2022

Source: fda.gov
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472


Holland & Barrett is recalling soya lecithin soft gel capsules because they contain peanuts which are not mentioned on the label. This means the product is a possible health risk for anyone with an allergy to peanuts.

The recalled products are:
- Ultra Soya Lecithin 1200mg (50... See More capsules)
- Ultra Soya Lecithin 1200mg (100 capsules)
- Ultra Soya Lecithin 1200mg (250 capsules)
- Mega Soya Lecithin 1325 mg (100 capsules)

Company name: Holland & Barrett
Product recalled: Ultra Soya Lecithin 1200mg, Ultra Soya Lecithin 1200mg, Ultra Soya Lecithin 1200mg, Mega Soya Lecithin 1325 mg
FSA Recall date: 11/07/2022

If you have bought the recalled products and have an allergy to peanuts, do not eat them. Instead return them to the store from where they were bought for a full refund.

In case you experienced harm from allergens or undeclared ingredients, 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.

Source: food.gov.uk
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77


Thornton, Colorado, Adam’s Polishes, LLC is voluntarily recalling lot 133475 of Adam’s Polishes Hand Sanitizer to the consumer level. FDA testing has found this lot to contain undeclared methanol. Adam’s Polishes is recalling 19 other lots in an abundance of caution. The hand sanitizer was distributed nationwide... See More in the USA to internet customers between June 2020 and March 2022. To date, Adam’s Polishes has not received any reports of injury, illness, or other adverse events related to this recall.

Risk Statement: Persons who accidently ingest (drink) these products are at risk for methanol poisoning. Substantial methanol ingestion can result in coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. This product is used as a hand sanitizer marketed to help decrease bacteria on the skin when soap and water are not available.

Adam’s Polishes Hand Sanitizer is packaged in 4oz., 8oz. 16oz., and one gallon bottles. These bottles are spray bottles for the 4oz, 8oz and 16oz and jugs for the gallon bottles. Lot numbers: 133470, 133471, 133472, 133473, 133474, 133475, 133476, 133477, 133478, 133479, 133480, 133481, 133482, 133483, 137731, 137732, 137733, 137734, 139322, 143327

Consumers who have any recalled Adam’s Polishes Hand Sanitizer products should immediately stop using the product and dispose of it in accordance with local regulations.

In case you experienced 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.

Company name: Adam’s Polishes, LLC
Brand name: Adam’s Polishes
Product recalled: Hand sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: November 07, 2022

Source: fda.gov
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