Drug Recalls

Here you'll find every drug recall the FDA has issued, including prescription medications, over-the-counter drugs, compounded pharmacy products, and dietary supplements. We've been tracking these since 2006 and our database updates several times a day so you're always looking at current information.

Drugs get recalled for a number of reasons: contamination during manufacturing, incorrect potency or dosage, failed quality testing (like dissolution or stability tests), sterility problems in injectable products, or labeling and packaging errors that could cause someone to take the wrong dose. If you find a product on this list that you use, please follow the instructions provided by the FDA to take the necessary precautions.

17,529 total recalls
1 this month

Showing 6441–6460 of 17,529 recalls

September 23, 2019· Macleods Pharma Usa Inc

Recalled Item: Pioglitazone Hydrochloride Tablets USP 15 mg

The Issue: Superpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 23, 2019· Unipharma, Llc.

Recalled Item: DrKids Himasal Natural Nasal Saline Solution

The Issue: CGMP Deviations: Recall as a precautionary measure due

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only Manufactured

The Issue: CGMP Deviations: Detection of a trace amount of

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 150mg 500 Capsules Rx Only Manufactured

The Issue: CGMP Deviations: Detection of a trace amount of

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 23, 2019· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Prednisolone Sodium Phosphate Oral Solution

The Issue: Failed Quality Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 23, 2019· Sandoz, Inc

Recalled Item: Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only Manufactured

The Issue: CGMP Deviations: Detection of a trace amount of

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 23, 2019· Unipharma, Llc.

Recalled Item: DrKids Children's Natural Cough Syrup English Ivy Leaf

The Issue: CGMP Deviations: Recall as a precautionary measure due

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 20, 2019· Akorn, Inc.

Recalled Item: Phenylephrine Hydrochloride Ophthalmic Solution

The Issue: Lack of Assurance of Sterility: Out of specification

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 19, 2019· Aurobindo Pharma USA Inc.

Recalled Item: Dextroamphetamine Sacharate

The Issue: Superpotent Drug: Amphetamine Mixed Salts 20mg have been

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium/ Hydrochlorothiazide Tablets

The Issue: CGMP Deviations: FDA lab confirmed presence of an

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
September 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium /Hydrochlorothiazide Tablets

The Issue: CGMP Deviations: FDA lab confirmed presence of an

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
September 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets

The Issue: CGMP Deviations: FDA lab confirmed presence of an

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
September 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets

The Issue: CGMP Deviations: FDA lab confirmed presence of an

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
September 18, 2019· Avella of Deer Valley, Inc. Store 38

Recalled Item: Povidone Iodine

The Issue: Lack of sterility assurance

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 18, 2019· GCP Laboratories Inc

Recalled Item: Major Infants' Gas Relief Drops

The Issue: Microbial Contamination of Non-Sterile Product

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 17, 2019· Akorn, Inc.

Recalled Item: Lidocaine Hydroclhoride Jelly USP

The Issue: cGMP Deviations: firm reported finding metal particulate matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 16, 2019· FITOTERAPIA USA, INC

Recalled Item: Mero Macho Artificially Flavored Passion Fruit Vitamin C Liquid Supplement

The Issue: Marketed without an approved NDA/ANDA: Product found to

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardTerminated
Refund
September 13, 2019· GUERBET LLC

Recalled Item: Sodium Chloride Injection USP 0.9%

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskTerminated
Refund
September 13, 2019· GUERBET LLC

Recalled Item: Optiray 320 (ioversol) Injection 68%

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 12, 2019· Spectrum Laboratory Products

Recalled Item: Fentanyl Citrate USP

The Issue: CGMP Deviations: Received notice from supplier that there

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund