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
0 this month

Showing 9021–9040 of 17,529 recalls

June 11, 2018· BioDiagnostic International

Recalled Item: Monsel's Solution (Ferric Subsulfate)

The Issue: CGMP Deviations: Products not manufactured under current good

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

Class II — Potential Health HazardTerminated
Refund
June 8, 2018· Qualgen, LLC

Recalled Item: ESTRADIOL 20mg PELLET

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskTerminated
Refund
June 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection

The Issue: Superpotent Drug: High out of specification assay value

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

Class II — Potential Health HazardTerminated
Refund
June 8, 2018· Qualgen, LLC

Recalled Item: TESTOSTERONE 200 mg PELLET

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskTerminated
Refund
June 8, 2018· Ingenus Pharmaceuticals Llc

Recalled Item: Irinotecan Hydrochloride Injection

The Issue: Superpotent Drug: High out of specification assay value

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

Class II — Potential Health HazardTerminated
Refund
June 7, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Maxzide-25 (Triamterene and hydrochlorothiazide) tablets

The Issue: Superpotent Drug: Composite assay results obtained during routine

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

Class III — Low RiskTerminated
Refund
June 6, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium Tc99m Medronate

The Issue: Lack of assurance of sterility: Technetium TC-99M Medronate

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2018· PharMEDium Services, LLC

Recalled Item: HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride

The Issue: Superpotent and Subpotent

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

Class II — Potential Health HazardTerminated
Refund
June 4, 2018· HOSPIRA INC, LAKE FOREST

Recalled Item: Naloxone Hydrochloride Injection

The Issue: Presence of Particulate Matter; Potential for particulate matter

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

Class I — Serious Health HazardTerminated
Refund
May 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of assurance of sterility: Bags have potential

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

Class II — Potential Health HazardTerminated
Refund
May 31, 2018· ICU Medical Inc

Recalled Item: 5% Dextrose Injection

The Issue: Lack of assurance of sterility: Bags have potential

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

Class II — Potential Health HazardTerminated
Refund
May 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of assurance of sterility: Bags have potential

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

Class II — Potential Health HazardTerminated
Refund
May 31, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of assurance of sterility: Bags have potential

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

Class II — Potential Health HazardTerminated
Refund
May 31, 2018· ICU Medical Inc

Recalled Item: 0.45% Sodium Chloride Injection

The Issue: Lack of assurance of sterility: Bags have potential

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

Class II — Potential Health HazardTerminated
Refund
May 31, 2018· Apotex Inc.

Recalled Item: Fluticasone propionate Nasal Spray

The Issue: Presence of foreign substance: glass particles

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

Class II — Potential Health HazardTerminated
Refund
May 30, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
May 29, 2018· Pharmaceutical Associates Inc

Recalled Item: Nystatin Oral Suspension

The Issue: Resuspension problems: Out of specification for appearance and

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

Class III — Low RiskTerminated
Refund
May 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: X-Jow (menthol USP) Pain Gel

The Issue: CGMP Deviations: products may be contaminated with bacteria

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

Class II — Potential Health HazardTerminated
Refund
May 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave 3 Step Shaving System

The Issue: CGMP Deviations: products may be contaminated with bacteria

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

Class II — Potential Health HazardTerminated
Refund
May 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid)

The Issue: CGMP Deviations: products may be contaminated with bacteria

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

Class II — Potential Health HazardTerminated
Refund