Subgenix cream, Tampa, FL, USA
3 weeks ago •reported by user-cmnfb465
I also received this cream today i did not order!!!
WishGarden Herbs Remedies Cord Care and Goldenseal Powder - recalled due to potential Cronobacter sakazakii contamination, USA
3 years ago •source www.fda.gov
Recall notice
United States
Company name: WishGarden Herbs, Inc.Brand name: WishGarden Herbal Remedies
Product recalled: Cord Care and Goldenseal Powder
Reason of the recall: Product may be contaminated with Cronobacter sakazakii
FDA Recall date: December 04, 2020
Recall details: Company Announcement WishGarden Herbs, Inc. is voluntarily recalling, to the consumer level, 14 lots of Cord Care and Goldenseal Powder products produced after 7/26/18 with expiration dates between 7/26/18 and 9/1/20. After receiving notice of a supply chain issue, WishGarden has determined these products were manufactured using ingredients potentially contaminated with Cronobacter sakazakii bacteria. Use of these products, when contaminated with this bacteria, may cause serious infections with severe outcomes, including death, especially in vulnerable patients with compromised immune systems and infants. Catherine Hunziker, WishGarden President, stated, “As a leading herbal product company for more than 40 years, we take the safety of our products seriously and we feel it is important to recall this product out of an abundance of caution. Consumer safety is our highest priority.”
Cord Care Powder is marketed to dry umbilical cords and is applied externally to skin. It is packaged in 1oz containers and labeled with UPC 6-56490-24730-4. The affected product lots are P227-P235. The lot and expiration date can be found below the label barcode. Goldenseal Powder is marketed as a drying powder applied externally to skin. It is packaged in 1oz containers and labeled with UPC 6-56490-64137-9. Affected product lots are P116-P120. The lot and expiration date can be found below the label barcode. These products were distributed nationwide in the USA through select practitioners.
WishGarden Herbs has notified its distributors and customers by phone, mail and email. Consumers who have purchased this recalled product should discontinue use immediately and not open any sealed packages. The product should be mailed directly to WishGarden Herbs corporate headquarters at 321 South Taylor Ave. Suite 100 Louisville, CO 80027 for a full refund. Consumers with questions regarding this recall can contact WishGarden Herbs by calling the company’s recall hotline at 720-889-9878 (M-F, 9am - 5pm MST) or Email: recall@wishgardenherbs.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on www.fda.gov
Source: FDA
303
Recent Interesting Reports
I am reporting a bottle of subgenix, New York, NY 10024, USA
2 weeks ago •reported by user-dfhq9323
I received a package that I did not order. A bottle of subgenix bioribose.
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Heathers Mottsy, Staten Island, NY, USA
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SKAM!!!!!!!!! I ordered a cross made out of horseshoes. Pieces were plastic and very small. Not cut right so nothing fit together. Worthless piece of junk! Had to try to put it together with many pieces and it is crooked and warped looking.
SCAM!!!!!!!!!!!!!!
SCAM!!!!!!!!!!!!!!
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1 week ago •reported by user-fwtc8752
It is a crystal ball that sits on a lighted base. Inside is something that looks like Saturn, the planet
from 2800 N Franklin Rd, Indianapolis, IN 46329
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Want a refund!, Deer Lodge, MT, USA
2 weeks ago •reported by user-hnvkg974
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Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
2 weeks 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
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
303
I received a ring instead of clothes, Taupō 3330, New Zealand
1 week ago •reported by user-jttn3275
I ordered from the company GRA very confused.
Ordered from a clothing company and instead of sending me clothes they sent me a Dimond ring? Looks very fake. The company name is GRA and on the card they sent it says they have a certificate but doesn’t …
Ordered from a clothing company and instead of sending me clothes they sent me a Dimond ring? Looks very fake. The company name is GRA and on the card they sent it says they have a certificate but doesn’t …
look legit turns out this happend to heaps of others very concerned should I be worried?
3
I bought Daisy by Marc Jacobs from Amazon and it was FAKE!!!, Greenwood, LA, USA
1 week ago •reported by user-pwgt4515
I bought Daisy by Marc Jacobs from Amazon and it was FAKE!!! I went and looked at the other perfume I have bought also and to my HORROR THOSE ARE FAKES AS WELL!!! BEWARE!!!
I checked my perfume that I paid a lot of money for from …
I checked my perfume that I paid a lot of money for from …
Amazon and it was a fake and upon checking my other perfume.. they are all fake!!!
| Symptoms: Other
9
I received a necklace from this address that I did not order, Ohio, USA
2 weeks ago •reported by user-fxnmz821
I ordered 2 mattresses on March 10- the tracking has not updated since the order but I was charged immediately for them. I go to the mailbox today and find a gold necklace that I have not ordered.
I have been waiting on 2 mattresses for nearly …
I have been waiting on 2 mattresses for nearly …
a month that does not have updated tracking information but I was charged for.
186
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