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 6281–6300 of 17,529 recalls

November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Kali Muriaticum 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Calcarea Fluorica 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Ferrum Phosphoricum 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Kali Sulphuricum 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Cell Salts Combination 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Calcarea Phosphorica 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: StellaLife VEGA Oral Gel Rinse (In equal parts of: Azadirachta Indica 1x

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Natrum Phosphoricum 6X Tablets

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Pareira (Brava) 1X Tincture

The Issue: CGMP Deviations: products were not manufactured under current

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

Class II — Potential Health HazardTerminated
Refund
November 6, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in

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

Class II — Potential Health HazardOngoing
Refund
November 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 300 mg

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in

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

Class II — Potential Health HazardOngoing
Refund
November 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Caspules 150 mg

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in

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

Class II — Potential Health HazardOngoing
Refund
November 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 150 mg

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in

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

Class II — Potential Health HazardOngoing
Refund
November 6, 2019· AuroMedics Pharma LLC

Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in

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

Class II — Potential Health HazardOngoing
Refund
November 6, 2019· Golden State Medical Supply Inc.

Recalled Item: GSMS: Ranitidine Capsules 150 mg

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
November 6, 2019· Golden State Medical Supply Inc.

Recalled Item: GSMS: Ranitidine Capsules 300 mg

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
November 4, 2019· Teva Pharmaceuticals USA, Inc.

Recalled Item: Valganciclovir Hydrochloride for Oral Solution

The Issue: Presence of foreign substance: Brown/black particles found during

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

Class II — Potential Health HazardTerminated
Refund
November 1, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP

The Issue: Presence of Foreign substance: identified as a dead

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

Class III — Low RiskTerminated
Refund
November 1, 2019· American Health Packaging

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP)

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
November 1, 2019· KVK-Tech, Inc.

Recalled Item: Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg

The Issue: Presence of Foreign Substance: Black particles were found

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

Class II — Potential Health HazardTerminated
Refund