Create a Report

Please provide report title

Please provide location

Make my report private

Please provide details

Alert regulators Alert business or product owner Get notifications for my case

Get alerts and updates for your case!

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

Please provide email or phone

Phone Number

Please provide email or phone

Show my report on homepage

We do not show your email or contact info

Skip this step

I agree to Terms & Conditions

Please accept our Terms & Conditions

Email or SMS copy of report

Enter below to get emailed a copy of your report, or sms a link to your report

Please provide email or phone

Phone number

Please provide email or phone

I agree to Terms & Conditions

Please accept our Terms & Conditions

Report by

Message us

Safety Reports: Recall

Updated: February 27, 2024 2:02 PM

Avanos Medical MIC* Gastric-Jejunal Feeding Tube Kits recalled due to potential lack of sterility, USA

9 months ago •source fda.gov • details

Recall notice

Avanos Medical, Inc. voluntarily recalled specific lots of MIC* Gastric – Jejunal Feeding Tube Kits on Jan. 16, 2024. These kits include Nurse Assist supplied syringes, pre-filled with sterile water, essential for inflating the retention balloon of the feeding tube. This recall initiated in direct response to… See more

#recall #medicaldevices #unitedstates

Avanos Medical MIC* Gastric-Jejunal Feeding Tube Kits recalled due to potential lack of sterility photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance, USA

9 months ago •source fda.gov • details

Recall notice

Brassica Pharma Pvt. Ltd. is voluntarily recalling the Eye Ointment products listed below with expiration dates ranging from February 2024 to September 2025. The products are being recalled due to a lack of sterility assurance. These products were distributed nationwide to wholesalers, retailers, and via the product… See more

#cvspharmacy #recall #walmart #drugs #unitedstates

Brassica Pharma Pvt. Ltd. Eye ointment products - recalled due to lack of sterility assurance photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander, USA

9 months ago •source fda.gov • details

Recall notice

Backstage Center is issuing a recall of approximately 280 Bottles of Alipotec Raiz de Tejocote, dietary supplements, that are labeled with the "Alipotec King" sticker. This recall is being initiated because FDA analysis found that the product contains toxic yellow oleander. The product has been exclusively distributed… See more

#amazon #dietarysupplements #recall #unitedstates

Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

H&Natural Brand Products - recalled due to Yellow oleander, USA

9 months ago •source fda.gov • details

Recall notice

San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native… See more

#amazon #walmart #dietarysupplements #recall #unitedstates

312

Helpful
Follow
Add my report
Share
- Copy link

Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage, USA

9 months ago •source fda.gov • details

Recall notice

Nordic Naturals is voluntarily recalling one lot of Nordic Naturals Baby’s Vitamin D3 Liquid. This recall is being conducted due to a manufacturing error that resulted in an elevated level of Vitamin D3 dosage or super potent dose. There have been no reports of adverse events to… See more

#dietarysupplements #recall #unitedstates

Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil, USA

9 months ago •source fda.gov • details

Recall notice

“Today The World” is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. FDA analysis has found the products to contain undeclared Tadalafil and Nortadalafil. Products were distributed online nationwide in the USA. To date, no… See more

#recall #drugs #unitedstates

Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Arize male enhancement capsules - recalled due to undeclared Nortadalafil, USA

9 months ago •source fda.gov • details

Recall notice

"Today The World” is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level. FDA analysis has found the products to contain undeclared Nortadalafil. The product was distributed online via their website in the USA. To date, no adverse events have been reported.… See more

#recall #drugs #unitedstates

Arize male enhancement capsules - recalled due to undeclared Nortadalafil photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack of sterility assurance, USA

9 months ago •source fda.gov • details

Recall notice

Nurse Assist, LLC voluntary product recall (which included products supplied to Cardinal Health used in Covidien and Cardinal Health™ brand kits and trays), Cardinal Health issued a medical device recall on December 5, 2023, for its Covidien and Cardinal Health™ brand urology and operating room-specific kits and… See more

#recall #medicaldevices #unitedstates

Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack of sterility assurance photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence, USA

9 months ago •source fda.gov • details

Recall notice

Insight Pharmaceuticals is voluntarily recalling two lots of TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid to the consumer level due to elevated levels of benzene. The affected TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid lots were distributed nationwide in the United States through… See more

#recall #drugs #unitedstates

TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine, USA

9 months ago •source fda.gov • details

Recall notice

Neptune Resources, LLC issues a voluntary recall of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets Products Due to the Presence of Tianeptine. The products were distributed nationwide in the USA to wholesale and retail customers. Neptune Resources LLC's distribution channels have not… See more

#recall #drugs #unitedstates