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 9761–9780 of 17,529 recalls

September 21, 2017· Medline Industries Inc

Recalled Item: Medline General Purpose Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline Incision Drainage Kit

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline GHS Suture Removal Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline Straight Suture Removal Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline Suture Removal Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Professional Hospital Supply Suture Removal Kit

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Liberator Medical Supply Catheter Insertion Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2017· Medline Industries Inc

Recalled Item: Medline All Purpose Instrument Tray

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine

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

Class II — Potential Health HazardTerminated
Refund
September 20, 2017· Natures Supplement

Recalled Item: Enhanced Vegetal Vigra 200 mg Capsules

The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found

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

Class I — Serious Health HazardTerminated
Refund
September 20, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Gel USP

The Issue: Cross contamination with other products: traces of Dapsone

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

Class III — Low RiskTerminated
Refund
September 20, 2017· Deserving Health International Corp

Recalled Item: Symbio Muc Eye

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
September 15, 2017· Gadget Island, Inc

Recalled Item: grande X 5800 capsule

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
September 15, 2017· Gadget Island, Inc

Recalled Item: FIFTY SHADES 6000 capsule

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
September 15, 2017· Gadget Island, Inc

Recalled Item: PapaZen 3300 capsule

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
September 15, 2017· Gadget Island, Inc

Recalled Item: RHINO 7 Platinum 5000

The Issue: Undeclared Active

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

Class I — Serious Health HazardTerminated
Refund
September 15, 2017· Becton Dickinson & Company

Recalled Item: ChloraPrep OneStep (Clear) (2% w/v chlorhexidine gluconate (CHG) and 70%

The Issue: Labeling; Label Mixup; the immediate package is labeled

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

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

Recalled Item: Intralipid 20%

The Issue: Temperature Abuse: A portion of this product lot

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

Class I — Serious Health HazardTerminated
Refund