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 9921–9940 of 17,529 recalls

August 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: G.A.C 25/100/250mg

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 15, 2017· Bella Pharmaceuticals, Inc.

Recalled Item: Calcium chloride 10%

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
August 15, 2017· Amphastar Pharmaceuticals, Inc.

Recalled Item: Ketorolac Tromethamine Injection

The Issue: Crystallization: Particulate matter (Ketorolac Calcium Salt) was observed

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

Class II — Potential Health HazardTerminated
Refund
August 11, 2017· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Phentermine Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Fentanyl 10 mcg in 0.9% Sodium Chloride 1 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Neostigmine Methylsulfate 5 mg/5 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Succinylcholine chloride 100 mg in 5 mL syringe

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Norepinephrine 8 mg in dextrose 5% 250 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Amiodarone 900 mg in dextrose 5% 500 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Morphine 50 mg in 0.9% Sodium Chloride 5 mL PCA

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Phenylephrine 1000 mcg in 0.9% Sodium Chloride 10 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Oxytocin 30 units in 0.9% Sodium Chloride 500 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: Fentanyl 2 mcg/mL and ropivacaine 0.2% in 0.9% Sodium Chloride 150 mL

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· SSM Health Care St. Louis DBA SSM St. Clare Health Center

Recalled Item: HYDROmorphone 10 mg in 0.9% Sodium Chloride 50 mL PCA

The Issue: Lack of sterility assurance: Microbial growth detected during

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· Premier Pharmacy Labs Inc

Recalled Item: Neostigmine Methylsulfate (single dose syringe) 1 mg per mL 5

The Issue: Stability Date Doesn't Support Expiry: labeling error indicating

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

Class II — Potential Health HazardTerminated
Refund
August 10, 2017· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Amoxicillin and Clavulanate Potassium for Oral Suspension

The Issue: Foreign Object Contamination

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

Class II — Potential Health HazardTerminated
Refund
August 7, 2017· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets

The Issue: Labeling: Label mix-up, the product labeled as Pravastatin

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

Class I — Serious Health HazardTerminated
Refund
August 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 4, 2017· Pfizer Inc.

Recalled Item: Quillivant XR methylphenidate HCl

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
August 4, 2017· Degasa Sa De Cv

Recalled Item: Povidone Iodine

The Issue: Labeling: Label mix-up. Finished product Povidone iodine 7.5%

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

Class II — Potential Health HazardTerminated
Refund