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Safety Reports: Drugs

Updated: September 5, 2023 11:01 AM

Real Time Reports

Recall notice

WEFUN Capsules - recalled due to Undeclared Sildenafil, USA

2 years ago •source fda.gov • details

Hua Da Trading Inc dba Wefun Inc. is voluntarily recalling 300 Boxes of WEFUN Capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) inhibitor found in FDA-approved products for the… See more

#drugs #recall #unitedstates

Recalls WEFUN Capsules - recalled due to Undeclared Sildenafil Hua Da Trading Inc dba Wefun Inc. is voluntar... photo #1

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Recall notice

Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up, USA

2 years ago •source fda.gov • details

Marlex Pharmaceuticals, Inc. is voluntarily recalling one lot of Digoxin Tablets USP, 0.125mg and one lot of Digoxin Tablets USP, 0.25mg to the consumer level due to Label Mix-Up. Bottles of Digoxin Tablets, USP 0.125mg s are incorrectly labeled and contain Digoxin Tablets USP, 0.25mg Tablets. Bottles… See more

#recall #drugs #unitedstates

Recalls Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up Marlex Pharmaceuticals, In... photo #1

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Recall notice

Dr. Berne's MSM drops and Mist - recalled due to Bacterial & Fungal Contamination, USA

2 years ago •source fda.gov • details

Dr. Berne's Whole Health Products is voluntarily recalling all lots of MSM DROPS 5%,15% Solution, Dr. Berne's Organic Castor Oil Eye Drops and Dr. Berne's MSM MIST 15% Solution to the consumer level. FDA analysis has found one lot (lot 6786) of Dr. Berne's MSM DROPS 5%… See more

#recall #drugs #unitedstates

Recalls Dr. Berne’s MSM drops and Mist - recalled due to Bacterial & Fungal Contamination Dr. Berne’s Whole... photo #1

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Recall notice

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

2 years ago •source fda.gov • details

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

#drugs #recall #unitedstates

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

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Recall notice

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

2 years ago •source accessdata.fda.gov • details

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

#drugs #recall #california #unitedstates

Recalls Food Research International supplements - recalled due to E. Coli FDA announced the recall of 2975 b... photo #1

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Recall notice

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

2 years ago •source fda.gov • details

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

#recall #drugs #unitedstates

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

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

2 years ago •reported by user-tjbbr958 • 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.

#drugs #walgreens #atlanta #georgia #unitedstates

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Recall notice

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

2 years ago •source gov.uk • details

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

#drugs #recall #unitedkingdom

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

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Recall notice

Cipla Albuterol Sulfate Inhalation Aerosol- recalled due to Failure to deliver the recommended dose, USA

2 years ago •source fda.gov • details

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

#recall #drugs #unitedstates

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

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Recall notice

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

2 years ago •source fda.gov • details

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

#recall #drugs #unitedstates

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

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Safety Reports: Drugs

Real Time Reports

WEFUN Capsules - recalled due to Undeclared Sildenafil, USA

Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up, USA

Dr. Berne's MSM drops and Mist - recalled due to Bacterial & Fungal Contamination, USA

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- recalled due to Failure to deliver the recommended dose, USA

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

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