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 9801–9820 of 17,529 recalls

September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 500 mL Lactated Ringer's Injection

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL bag

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 1000 mL Lactated Ringer's Injection

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL 5% Dextrose/Lactated Ringer's

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag Rx Only

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 15 units added to 250 mL Lactated Ringer's Injection USP in 250 mL bag

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
September 1, 2017· Pfizer Inc.

Recalled Item: Sterile Water for Injection

The Issue: Non-Sterility: cracked or chipped glass at the neck

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

Class II — Potential Health HazardTerminated
Refund
August 31, 2017· Amneal Pharmaceuticals LLC

Recalled Item: Fosphenytoin Sodium Injection

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardTerminated
Refund
August 30, 2017· Pfizer Inc.

Recalled Item: Vancomycin Hydrochloride for Injection

The Issue: Presence of Particulate Matter: glass particulate found in

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

Class I — Serious Health HazardTerminated
Refund
August 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours

The Issue: Defective Delivery System: Products no longer meet the

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

Class II — Potential Health HazardTerminated
Refund
August 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours

The Issue: Defective Delivery System: Products no longer meet the

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

Class II — Potential Health HazardTerminated
Refund
August 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours

The Issue: Defective Delivery System: Products no longer meet the

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

Class II — Potential Health HazardTerminated
Refund
August 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours

The Issue: Defective Delivery System: Products no longer meet the

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

Class II — Potential Health HazardTerminated
Refund