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
2 this month

Showing 3821–3840 of 17,529 recalls

January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Back Relief II (Acetaminophen 200 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: 3-Component Cold Tabs (Acetaminophen 325 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Coated APAP 500 mg caplet (Acetaminophen 500 mg) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Coated APAP 325mg (Acetaminophen 325 mg) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· AuroMedics Pharma LLC

Recalled Item: Polymyxin B for Injection USP

The Issue: Presence of Particulate Matter; product complaint of hair

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

Class I — Serious Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Coated APAP 325 mg Phenyl HCl 5 mg tablet (Acetaminophen 325 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Trial Antacid Tablet (Calcium Carbonate 420 mg) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Legatrin (Acetaminophen 500 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Cherry Antacid Tablet (Calcium Carbonate 420 mg) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Normed Fem Tablet (Acetaminophen 325 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: 4-Component Cold Tabs (Acetaminophen 325 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: HPC Tablet (Acetaminophen 110 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Coated Back Relief Tablet (Acetaminophen 250 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Coated Phenylephrine HCl 5mg Tablet (Phenylephrine HCl 5mg ) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Peppermint Antacid tablet (Calcium Carbonate 420 mg) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: DBI Magnums Tablet (Caffeine 200 mg) 100 and 500 count

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Extra-Strength Unaspirin caplet (Acetaminophen 500 mg) Bulk Container

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Pain Aid PMF Caplet (Acetaminophen 500 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Kramer Novis Tusicof Caplet (Guaifenesin 400 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
January 26, 2022· ULTRAtab Laboratories, Inc.

Recalled Item: Ephedrine 25 Guaifenesin 200 Tablet (Ephedrine HCl 25 mg

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund