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 3181–3200 of 17,529 recalls

June 7, 2022· Plastikon Healthcare LLC

Recalled Item: GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL

The Issue: CGMP Deviations: products manufactured under conditions which reflect

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

Class II — Potential Health HazardTerminated
Refund
June 7, 2022· Plastikon Healthcare LLC

Recalled Item: Magnesium Hydroxide 2400 mg

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardTerminated
Refund
June 7, 2022· Plastikon Healthcare LLC

Recalled Item: GUAIFENESIN AND DEXTROMETHORPHAN 200-20 mg/10 mL

The Issue: CGMP Deviations: products manufactured under conditions which reflect

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

Class II — Potential Health HazardTerminated
Refund
June 6, 2022· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be

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

Class II — Potential Health HazardTerminated
Refund
June 6, 2022· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be

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

Class II — Potential Health HazardTerminated
Refund
June 6, 2022· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be

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

Class II — Potential Health HazardTerminated
Refund
June 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection

The Issue: CGMP Deviations: Manufacturing deviations were reported due to

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

Class II — Potential Health HazardTerminated
Refund
June 3, 2022· Akorn, Inc.

Recalled Item: Olopatadine HCl

The Issue: Failed impurity/degradation specifications: Out of specification for 2-HMP

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

Class III — Low RiskTerminated
Refund
June 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection

The Issue: CGMP Deviations: lots made with same active pharmaceutical

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

Class II — Potential Health HazardTerminated
Refund
June 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Clonazepam Orally Disintegrating Tablets

The Issue: Failed Tablet/Capsule Specification; oversized tablet found in a

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

Class II — Potential Health HazardTerminated
Refund
May 26, 2022· Amazon.com, Inc.

Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardTerminated
Refund
May 26, 2022· Amazon.com, Inc.

Recalled Item: Ortiga mas Ajo Rey con Omega 3

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardTerminated
Refund
May 26, 2022· Amazon.com, Inc.

Recalled Item: Artri King con Ortiga y Omega 3 tablets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardTerminated
Refund
May 24, 2022· Grato Holdings, Inc.

Recalled Item: Homeopathic EarAche 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
May 24, 2022· Walmart Inc

Recalled Item: Artri Ajo King con Ortiga y Omega 3 Tablets

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were

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

Class II — Potential Health HazardCompleted
Refund
May 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were

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

Class II — Potential Health HazardCompleted
Refund
May 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardCompleted
Refund
May 24, 2022· Grato Holdings, Inc.

Recalled Item: Homeopathic EarAche Ear 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
May 24, 2022· US Specialty Formulations LLC

Recalled Item: B-Complex + Chromic Chloride (Choline Chloride 3%

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
May 24, 2022· US Specialty Formulations LLC

Recalled Item: Ethanol for Injection 95%

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund