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 6781–6800 of 17,529 recalls

July 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil 30 mg/2 mg/30 mcg/mL Injectable

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Acetylcysteine 2% Otic Drop

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil/Atropine 30 mg/2 mg/50 mcg/0.15 mg/mL...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil - 30 mg/1 mg/10 mcg/mL Injectable

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 mcg/mL Injectable

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Papaverine/Phentolamine 30 mg/1 mg/mL Injectable

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Dexamethasone Sodium Phosphate PF 24 mg/mL Injection

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Gentamicin (GU) Irrigation 240 mg/500 mL Solution

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 22, 2019· Wise Pharmacy

Recalled Item: Alprostadil 100 mcg/mL Injectable

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
July 19, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP

The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of

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

Class II — Potential Health HazardTerminated
Refund
July 19, 2019· Dercher Enterprises, Inc., DBA Gordon Laboratories

Recalled Item: MONSEL'S (Ferric Subsulfate) Solution

The Issue: Microbial Contamination of Non-Sterile Products and Superpotent Drug:

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

Class II — Potential Health HazardTerminated
Refund
July 19, 2019· Ascend Laboratories LLC

Recalled Item: Atorvastatin Calcium Tablet USP 80 mg

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 18, 2019· Ucb, Inc

Recalled Item: Keppra (levetiracetam) 1000 mg tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 18, 2019· Preferred Pharmaceuticals, Inc

Recalled Item: Neomycin Sulfate 3.5 mg/Polymyxin B Sulfate 10

The Issue: CGMPs Deviations: Insufficient Quality Assurance controls over critical

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

Class II — Potential Health HazardTerminated
Refund
July 18, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC

The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was

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

Class III — Low RiskTerminated
Refund
July 18, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP

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
July 17, 2019· Macleods Pharma Usa Inc

Recalled Item: Tamsulosin Hydrochloride Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 17, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP

The Issue: Presence of Foreign Substance; Product complaints received related

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

Class II — Potential Health HazardTerminated
Refund
July 17, 2019· ImprimisRx NJ

Recalled Item: Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
July 17, 2019· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund