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 6381–6400 of 17,529 recalls

October 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-MuSkel-Neural

The Issue: Lack of Assurance of Sterility: products manufactured in

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

Class II — Potential Health HazardTerminated
Refund
October 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Relief +

The Issue: Lack of Assurance of Sterility: products manufactured in

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

Class II — Potential Health HazardTerminated
Refund
October 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Systemic Detox

The Issue: Lack of Assurance of Sterility: products manufactured in

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

Class II — Potential Health HazardTerminated
Refund
October 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Neuro

The Issue: Lack of Assurance of Sterility: products manufactured in

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

Class II — Potential Health HazardTerminated
Refund
October 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Male+

The Issue: Lack of Assurance of Sterility: products manufactured in

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

Class II — Potential Health HazardTerminated
Refund
October 15, 2019· 8046255 Canada Inc. DBA Viatrexx

Recalled Item: Viatrexx-Adipose

The Issue: Lack of Assurance of Sterility: products manufactured in

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

Class II — Potential Health HazardTerminated
Refund
October 11, 2019· X-Gen Pharmaceuticals Inc.

Recalled Item: Levetiracetam Injection

The Issue: Labeling: Incorrect or Missing Package Insert - the

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

Class III — Low RiskTerminated
Refund
October 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardTerminated
Refund
October 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Sermorelin w/ GHRP2 3 mg For injection

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardTerminated
Refund
October 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Chorionic Gonadotropin 11

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardTerminated
Refund
October 10, 2019· Innoveix Pharmaceuticals Inc

Recalled Item: Lyophilized Human Chorionic Gonadotropin 5

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardTerminated
Refund
October 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl

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
October 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Bupivacaine HCl 0.125% in 0.9%

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardTerminated
Refund
October 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate (2 mcg/mL)* & Bupivacaine HCl 0.0625 in 0.9%

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardTerminated
Refund
October 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: del Nido Cardioplegia Solution

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
October 9, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Fentanyl Citrate 2 mcg/mL* & Ropivacaine HCl 0.1% in 0.9%

The Issue: GMP Deviations: potential glass contamination

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

Class II — Potential Health HazardTerminated
Refund
October 9, 2019· Ingenus Pharmaceuticals Llc

Recalled Item: Leucovorin Calcium Injection

The Issue: Crystallization: Presence of particulate matter identified as API

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

Class II — Potential Health HazardTerminated
Refund
October 7, 2019· Mylan Laboratories Limited (Sterile Products Division)

Recalled Item: Rifampin for Injection

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 4, 2019· KVK-Tech, Inc.

Recalled Item: Methylphenidate Hydrochloride Oral Solution 5mg per 5mL

The Issue: Presence of Foreign Substance; Fiber particles

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

Class III — Low RiskTerminated
Refund
October 2, 2019· Pfizer Inc.

Recalled Item: 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection

The Issue: Lack of Assurance of Sterility: Bag has the

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

Class II — Potential Health HazardTerminated
Refund