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 9641–9660 of 17,529 recalls

November 3, 2017· Ridge Properties, LLC

Recalled Item: Extra Strength PreTAT by TAT BALM Gel

The Issue: GMP Deviations: inadequate manufacturing control processes

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

Class II — Potential Health HazardTerminated
Refund
November 3, 2017· Ridge Properties, LLC

Recalled Item: Extra Strength Naturally HL Hemorrhoid Numbing Spray with Lidocaine

The Issue: GMP Deviations: inadequate manufacturing control processes

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

Class II — Potential Health HazardTerminated
Refund
October 30, 2017· Pharmedium Services, LLC

Recalled Item: ePHEDrine Sulfate In 0.9% Sodium Chloride

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
October 30, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol

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
October 30, 2017· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Meclizine hydrochloride tablets USP

The Issue: Marketed without an approved NDA/ANDA: Bottles were released

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

Class III — Low RiskTerminated
Refund
October 27, 2017· Fresenius Kabi USA, LLC

Recalled Item: Midazolam Injection

The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam

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

Class I — Serious Health HazardTerminated
Refund
October 25, 2017· Fagron, Inc

Recalled Item: Estriol

The Issue: cGMP Deviations: lack of quality assurance at the

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

Class II — Potential Health HazardTerminated
Refund
October 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Dutasteride and Tamsulosin HCl Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 24, 2017· Ace Surgical Supply Co., Inc.

Recalled Item: Succinylcholine 20 MG/ML INJ (QUELICIN)

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

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

Class II — Potential Health HazardTerminated
Refund
October 24, 2017· Amerisource Health Services

Recalled Item: Paroxetine Tablets

The Issue: Presence of Foreign Tablets/Capsules

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

Class II — Potential Health HazardTerminated
Refund
October 20, 2017· Pfizer Inc.

Recalled Item: Zoloft (sertraline HCl) tablets 25 mg* 30-count bottle

The Issue: SUPERPOTENT: Weight variations resulting in tablets that are

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

Class II — Potential Health HazardTerminated
Refund
October 20, 2017· Pfizer Inc.

Recalled Item: diphenoxylate hydrochloride and atropine sulfate tablets

The Issue: SUPERPOTENT: Weight variations resulting in tablets that are

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

Class I — Serious Health HazardTerminated
Refund
October 19, 2017· Allergan Sales, LLC

Recalled Item: Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 19, 2017· Allergan Sales, LLC

Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01%

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: fentaNYL as citrate 2 mcg / mL

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: fentanyl as citrate 2 mcg per mL BUPIvacaine HCl 0.125%

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: morphine sulfate 1 mg per mL in 0.9% Sodium Chloride

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: SUCcinylcholine 20 mg per mL

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund