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 10141–10160 of 17,529 recalls

May 18, 2017· SCA Pharmaceuticals

Recalled Item: MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable

The Issue: Lack of assurance of sterility: Product bags leaking

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

Class II — Potential Health HazardTerminated
Refund
May 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable

The Issue: Lack of assurance of sterility: Product bags leaking

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

Class II — Potential Health HazardTerminated
Refund
May 18, 2017· SCA Pharmaceuticals

Recalled Item: morphine sulfate in 0.9% Sodium Chloride injectable

The Issue: Lack of assurance of sterility: Product bags leaking

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

Class II — Potential Health HazardTerminated
Refund
May 18, 2017· SCA Pharmaceuticals

Recalled Item: ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable

The Issue: Lack of assurance of sterility: Product bags leaking

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

Class II — Potential Health HazardTerminated
Refund
May 18, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCL in 0.9% Sodium Chloride injectable

The Issue: Lack of assurance of sterility: Product bags leaking

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

Class II — Potential Health HazardTerminated
Refund
May 18, 2017· Forest Laboratories, LLC

Recalled Item: Saphris 10 mg (asenapine) sublingual tablets

The Issue: Labeling; Label Mixup; blister lidding foil and shell-pack

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

Class II — Potential Health HazardTerminated
Refund
May 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable

The Issue: Lack of assurance of sterility: Product bags leaking

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

Class II — Potential Health HazardTerminated
Refund
May 17, 2017· X-Gen Pharmaceuticals Inc.

Recalled Item: Nystatin Topical Powder

The Issue: Presence of Foreign Substance: potential presence of plastic

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

Class II — Potential Health HazardTerminated
Refund
May 17, 2017· VistaPharm, Inc.

Recalled Item: Nystatin Oral Suspension

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
May 16, 2017· Lupin Limited (Unit 1)

Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02

The Issue: Contraceptive Tablets Out of Sequence- First 4 pills

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

Class I — Serious Health HazardTerminated
Refund
May 16, 2017· GlaxoSmithKline, LLC

Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation

The Issue: Defective Delivery System: Elevated number of units with

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

Class II — Potential Health HazardOngoing
Refund
May 15, 2017· Baxter Healthcare Corporation

Recalled Item: Milrinone Lactate in 5% Dextrose Injection

The Issue: Lack of assurance of sterility: customer complaints received

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2017· Baxter Healthcare Corporation

Recalled Item: Fluconazole Injection

The Issue: Lack of assurance of sterility: customer complaints received

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

Class II — Potential Health HazardTerminated
Refund
May 11, 2017· AtHome Medical, Inc.

Recalled Item: Oxygen Liquid USP UN 1073

The Issue: GMP Deviations: The firm does not include an

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

Class II — Potential Health HazardTerminated
Refund
May 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
May 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
May 10, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Divalproex Sodium Delayed Release Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
May 9, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Montelukast Sodium Oral Granules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
May 9, 2017· Strides Pharma INC

Recalled Item: Benzonatate capsules

The Issue: Failed Stability Specifications: Out of Specification results obtained

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

Class III — Low RiskTerminated
Refund
May 8, 2017· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCORTISONE LOTION

The Issue: Superpotent Drug: above specification for the assay

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

Class III — Low RiskTerminated
Refund