Create a Report

Please provide report title

Please provide location

Please provide details

Make my report private

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

Safety Reports: Recall

Updated: June 1, 2022 8:00 PM

Real Time Reports

Recall notice

Walmart Inc. Joint supplements - recalled due to contains diclofenac, USA

3 years ago •source fda.gov • details

Walmart Inc. is voluntarily recalling all lots of Artri Ajo King Joint Supplements sold by Innovacion Naturals and PDX Supply Warehouse LLC on Walmart.com and shipped by Walmart to the consumer level. FDA laboratory analysis confirmed that Artri Ajo King Omega 3 Joint Support Supplement with LOTE… See more

#recall #drugs #walmart #unitedstates #ro-tel

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Botanic Choice Senna Softgels - recalled due to Undeclared peanuts, USA

3 years ago •source fda.gov • details

Indiana Botanic Gardens Inc. of Indiana, is recalling its 30-count bottles of Botanic Choice brand Prune & Senna Softgels because they may contain undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. No illnesses… See more

#peanutallergy #vitamins #raw #recall #unitedstates #indian #sub #peanuts

Recalls Botanic Choice Senna Softgels - recalled due to Undeclared peanuts Indiana Botanic Gardens Inc. of I... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Alterna Bond Repair Leave-in Heat Protection Spray - recalled due to potential Burkholderia cepacia complex contamination, USA

3 years ago •source fda.gov • details

Henkel Corporation (“Henkel”) is voluntarily recalling 180 bottles of its 4.2 ounce Alterna Bond Repair Leave-in Heat Protection Spray, because it has the potential to be contaminated with Burkholderia cepacia complex (Bcc), which poses little medical risk to healthy people, but can cause an increased risk for… See more

#recall #cosmetics #unitedstates #specialk

Recalls Alterna Bond Repair Leave-in Heat Protection Spray - recalled due to potential Burkholderia cepacia... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Medical marijuana products - recalled due to failed tests for mold, E. coli, yeast, and salmonella, Oklahoma, USA

3 years ago •source poncacitynow.com • details

The Oklahoma Medical Marijuana Authority has recalled 99 medical marijuana products after samples failed tests for mold, E. coli, yeast, and salmonella.

During OMMA's routine inspections and reviewing of records, it discovered results not accurately reported by the testing lab. See images for the list of the… See more

#marijuana #drugs #recall #oklahoma #unitedstates #salmon #ro-tel

Recalls Medical marijuana products - recalled due to failed tests for mold, E. coli, yeast, and salmonella T... photo #1

40

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Teva Anagrelide Capsules - recalled due to Dissolution Test Failure, USA

3 years ago •source fda.gov • details

Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. No other… See more

#blood #recall #drugs #unitedstates #ro-tel

Recalls Teva Anagrelide Capsules - recalled due to Dissolution Test Failure Teva Pharmaceuticals USA has ini... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

NaturesPlus Keto Living Sugar Control Capsules - recalled due to undeclared Gluten, USA

3 years ago •source fda.gov • details

Natural Organics, Inc., is voluntarily recalling four lots of NaturesPlus Keto Living Sugar Control Capsules 90 count, because it was found to contain gluten. People who have allergies to wheat or gluten run the risk of serious or life-threatening allergic reactions if they consume these products. There… See more

#protein #raw #recall #unitedstates #sub #ham #orange #sugar

Recalls NaturesPlus Keto Living Sugar Control Capsules - recalled due to undeclared Gluten Natural Organics... photo #1

312

Helpful
Follow
Add my report
Share
- Copy link

I was sold a recalled product, Nashville, TN, USA

3 years ago •reported by user-rkfg1231 • details

I ordered a sex performance booster online, it was recalled due to adverse effects. I had a stroke later the same day. It is "MegMen performance booster ". Im in Nashville, the company that sold me the recalled over the counter drug is in New York. According… See more

#drugs #recall #nashville #tennessee #unitedstates

242

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Philips Respironics V60/V60 Plus, and V680 - recalled due to potential power supply issue, USA

3 years ago •source fda.gov • details

Royal Philips (NYSE: PHG, AEX: PHIA), today announced that its subsidiary Philips Respironics is notifying customers of its V60/V60 Plus and V680 ventilators about a potential issue with the electrical circuit in these ventilators that controls the 35V power supply to the ventilator and alarm. Philips Respironics… See more

#recall #medicaldevices #unitedstates #sub #ro-tel

312

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Pfizer Accupril (Quinapril HCl) tablets - recalled due to Due to N-Nitroso-Quinapril, USA

3 years ago •source fda.gov • details

Pfizer is voluntarily recalling five (5) lots of Accupril (Quinapril HCl) tablets distributed by Pfizer to the patient (consumer/user) level due to the presence of a nitrosamine, Nnitroso-quinapril, observed in recent testing above the Acceptable Daily Intake (ADI) level.

Nitrosamines are common in water and foods, including… See more

#blood #recall #drugs #unitedstates #vegetable #meat #ro-tel

Recalls Pfizer Accupril (Quinapril HCl) tablets - recalled due to Due to N-Nitroso-Quinapril Pfizer is volun... photo #1

313

Helpful
Follow
Add my report
Share
- Copy link

Recall notice

Babyganics Chamomile verbena bubble bath - recalled due to presence of a bacterium, USA

3 years ago •source fda.gov • details

Babyganics is voluntarily recalling two lots of 20-ounce bottles of babyganics® 20oz chamomile verbena bubble bath, due to the presence of the bacterium Pluralibacter gergoviae. The products were sold in the last two months only at select retailers in the U.S.

During internal testing related to product… See more

#recall #cosmetics #unitedstates #sub #ham

Recalls Babyganics Chamomile verbena bubble bath - recalled due to presence of a bacterium Babyganics is vol... photo #1

312 1 Share

Helpful
Follow
Add my report
Share
- Copy link

Create a Report

Get alerts and updates for your case!

Add photos or video

Email or SMS copy of report

Thank you for your report!

Safety Reports: Recall

Real Time Reports

Walmart Inc. Joint supplements - recalled due to contains diclofenac, USA

Botanic Choice Senna Softgels - recalled due to Undeclared peanuts, USA

Alterna Bond Repair Leave-in Heat Protection Spray - recalled due to potential Burkholderia cepacia complex contamination, USA

Medical marijuana products - recalled due to failed tests for mold, E. coli, yeast, and salmonella, Oklahoma, USA

Teva Anagrelide Capsules - recalled due to Dissolution Test Failure, USA

NaturesPlus Keto Living Sugar Control Capsules - recalled due to undeclared Gluten, USA

I was sold a recalled product, Nashville, TN, USA

Philips Respironics V60/V60 Plus, and V680 - recalled due to potential power supply issue, USA

Pfizer Accupril (Quinapril HCl) tablets - recalled due to Due to N-Nitroso-Quinapril, USA

Babyganics Chamomile verbena bubble bath - recalled due to presence of a bacterium, USA

I have a concern about this report:

Resolve my concern fast!

Thanks for your feedback!

Notify me when my concern is resolved

Thanks for your feedback!

Create a Report

Get alerts and updates for your case!

Add photos or video

Email or SMS copy of report

Thank you for your report!

Real Time Reports

Country

Type

Date

I have a concern about this report:

Resolve my concern fast!

Thanks for your feedback!

Notify me when my concern is resolved

Thanks for your feedback!