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

Safety Reports: Drugs

Updated: August 25, 2023 2:01 PM

Real Time Reports

Furst-McNess Company 18% Goat Starter Medicated Feed - recalled due to Elevated level of Monovet 90 (monensin), Wisconsin, United States

1 year ago •source fda.gov • details

Recall notice

Furst-McNess Company of Rockford, IL is recalling 18% Goat Starter feed due to an elevated level of Monovet® 90 (monensin). Monensin is an FDA-approved drug for use in certain animal feeds. However, if the feed contains excessive amounts of the drug, the feed can cause monensin toxicity… See more

#recall #drugs #unitedstates

Furst-McNess Company 18% Goat Starter Medicated Feed - recalled due to Elevated level of Monovet 90 (monensin) photo #1

Helpful
Follow
Add my report
Share
- Copy link

Food Research International supplements - recalled due to E. Coli, California, USA

1 year ago •source accessdata.fda.gov • details

Recall notice

FDA announced the recall of 2975 bottles of Food Research International Uro Kid Support Capsules and Serious Brain Enhancer Capsules by Global Vitality Inc. due to potential E. Coli contamination. These products were distributed to a single consignee in California. Details about the consignee were not provided.… See more

#recall #drugs #california #unitedstates #e.coli

Food Research International supplements - recalled due to E. Coli photo #1

Helpful
Follow
Add my report
Share
- Copy link

Lupin Tydemy oral contraceptive - recalled due to Out of Specification Results, USA

1 year ago •source fda.gov • details

Recall notice

Lupin Pharmaceuticals Inc. (Lupin) is voluntarily recalling two (2) lots of Tydemy (Drospirenone, Ethinyl Estradiol and Levomefolate Calcium Tablets 3mg/0.03mg/0.451 mg and Levomefolate Calcium Tablets 0.451 mg) to the patient (consumer/user) level due to out of specification (OOS) test results at the 12-month stability time point. Specifically,… See more

#drugs #recall #unitedstates

Lupin Tydemy oral contraceptive - recalled due to Out of Specification Results photo #1

Helpful
Follow
Add my report
Share
- Copy link

Walgreens, Atlanta, GA, USA, Atlanta, GA, USA

1 year ago • details

I’ve been taking a bad batch of vancomyosin, 125 mg. The capsules contain no powder. They contain a hard concrete like substance. They came from India. I got them there in Atlanta Georgia.

#walgreens #drugs #atlanta #georgia #unitedstates

Helpful
Follow
Add my report
Share
- Copy link

Labetalol 200mg Tablets - recalled due to an error on the foil blister packaging, UK

1 year ago •source gov.uk • details

Recall notice

Tillomed Laboratories Limited is recalling one batch of Labetalol 200mg Tablets due to an error on the foil blister packaging. The incorrect aluminium foil blister packaging states Labetalol 100mg Tablets, however it should be labelled as Labetalol 200mg Tablets. This error has occurred at the primary packing… See more

#recall #drugs #unitedkingdom

Labetalol 200mg Tablets - recalled due to an error on the foil blister packaging photo #1

Helpful
Follow
Add my report
Share
- Copy link

Cipla Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 MI)- recalled due to Failure to deliver the recommended dose, USA

1 year ago •source fda.gov • details

Recall notice

Cipla Limited (BSE: 500087; NSE: CIPLA EQ; and hereafter referred to as "Cipla"), today announced that its wholly-owned subsidiary Cipla US is voluntarily recalling six batches of Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 Metered Inhalation) manufactured in November 2021 to the consumer level due to Failure… See more

#drugs #recall #unitedstates

Cipla Albuterol Sulfate Inhalation Aerosol- recalled due to Failure to deliver the recommended dose photo #1

Helpful
Follow
Add my report
Share
- Copy link

Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up, USA

1 year ago •source fda.gov • details

Recall notice

The Harvard Drug Group, LLC d/b/a Major Pharmaceutical and Rugby Laboratories is initiating a voluntary recall of a single lot of Dronabinol Capsules, USP, 2.5 mg and Ziprasidone Hydrochloride Capsules, 20 mg to the consumer level. The Harvard Drug Group, LLC received a customer complaint from a… See more

#drugs #recall #unitedstates

Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up photo #1

Helpful
Follow
Add my report
Share
- Copy link

G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging, Puerto Rico

2 years ago •source fda.gov • details

Recall notice

Novis PR LLC is voluntarily recalling Lot D20911 Exp 10/25 of G-Supress DX Pediatric Drops to the consumer level. Some cartons of the product have been found to contain incorrect product inside. Incorrect product inside is an anesthetic/analgesic and not a brand of Novis PR LLC. Lot… See more

#recall #drugs #puertorico

G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging photo #1

Helpful
Follow
Add my report
Share
- Copy link

Akorn human & animal drug products update - recalled due to discontinuation of the Quality program, USA

2 years ago •source fda.gov • details

Recall notice

The Akorn Trustee is initiating a voluntary recall of various within-expiry human and animal products as a result of the closures and discontinuation of the Quality activities of these marketed products. The discontinuation of the Quality program means the company will not be able to support or… See more

#drugs #recall #unitedstates

Akorn human & animal drug products update - recalled due to discontinuation of the Quality program photo #1

Helpful
Follow
Add my report
Share
- Copy link

Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead, USA

2 years ago •source fda.gov • details

Recall notice

Del Maguey Co., New York, NY is conducting a voluntary recall of certain ceramicware cups called copitas – small artisan cups traditionally used for drinking mezcal – because they may exceed FDA guidance levels for leachable lead. The copitas were distributed free-of-charge to consumers at retail locations,… See more

#drugs #recall #unitedstates

Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead photo #1

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: Drugs

Real Time Reports

Furst-McNess Company 18% Goat Starter Medicated Feed - recalled due to Elevated level of Monovet 90 (monensin), Wisconsin, United States

Food Research International supplements - recalled due to E. Coli, California, USA

Lupin Tydemy oral contraceptive - recalled due to Out of Specification Results, USA

Walgreens, Atlanta, GA, USA, Atlanta, GA, USA

Labetalol 200mg Tablets - recalled due to an error on the foil blister packaging, UK

Cipla Albuterol Sulfate Inhalation Aerosol, 90 mcg (200 MI)- recalled due to Failure to deliver the recommended dose, USA

Major Dronabinol and Ziprasidone Hydrochloride capsules- recalled due to labeling mix-up, USA

G-SUPRESS DX pediatric drops- recalled due to Incorrect Packaging, Puerto Rico

Akorn human & animal drug products update - recalled due to discontinuation of the Quality program, USA

Del Maguey Copitas-Artisan ceramicware cups - recalled due to exceed levels for leachable lead, 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!