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
2 this month

Showing 1581–1600 of 17,529 recalls

October 18, 2023· Integrity Bio-Chemicals LLC

Recalled Item: Integrity Biochem HSC 70-VA

The Issue: CGMP Deviation: Third party test results showing a

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2023· Exela Pharma Sciences LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection

The Issue: Presence of Particulate Matter: Silicone

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

Class I — Serious Health HazardOngoing
Refund
October 18, 2023· Integrity Bio-Chemicals LLC

Recalled Item: Integrity Biochem HSC 70-LM

The Issue: CGMP Deviation: Third party test results showing a

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2023· Integrity Bio-Chemicals LLC

Recalled Item: Integrity Biochem HSC70-LV

The Issue: CGMP Deviation: Third party test results showing a

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2023· Exela Pharma Sciences LLC

Recalled Item: Midazolam in 0.8% Sodium Chloride Injection 100 mg/100 mL (1mg/mL)

The Issue: Presence of Particulate Matter: Silicone

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

Class I — Serious Health HazardOngoing
Refund
October 18, 2023· VistaPharm LLC

Recalled Item: Sucralfate Oral Suspension

The Issue: Microbial Contamination of Non-Sterile Products: identified as Bacillus

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

Class I — Serious Health HazardTerminated
Refund
October 17, 2023· VistaPharm LLC

Recalled Item: Aminocaproic Acid Oral Solution

The Issue: Failed Excipient Specifications: high content of ethylene glycol

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

Class III — Low RiskTerminated
Refund
October 17, 2023· AbbVie Inc.

Recalled Item: Synthroid

The Issue: Labeling: Wrong Barcode- One (1) of every forty

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

Class III — Low RiskOngoing
Refund
October 16, 2023· Noah's Wholesale LLC

Recalled Item: THE ROCK

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 HazardOngoing
Refund
October 13, 2023· Dr. Reddy's Laboratories, Inc.

Recalled Item: Montelukast Sodium Tablets

The Issue: Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was

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

Class II — Potential Health HazardTerminated
Refund
October 5, 2023· Dollar Tree Distribution, Inc.

Recalled Item: Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail

The Issue: CGMP Deviations: OTC products were stored outside of

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

Class II — Potential Health HazardOngoing
Refund
October 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clinical TREAT Antifungal Powder

The Issue: CGMP deviations: the product was shipped from the

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

Class II — Potential Health HazardTerminated
Refund
October 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF

The Issue: Labeling: Not Elsewhere Classified

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

Class III — Low RiskTerminated
Refund
October 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF

The Issue: Labeling: Not Elsewhere Classified

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

Class III — Low RiskTerminated
Refund
October 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Oxytocin synthetic

The Issue: Labeling: Not Elsewhere Classified

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

Class III — Low RiskTerminated
Refund
October 4, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (SR)

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 3, 2023· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use...

The Issue: Subpotent: Failing Test Results for Epinephrine

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

Class III — Low RiskTerminated
Refund
October 2, 2023· Pfizer Inc.

Recalled Item: 2% Lidocaine HCl Injection

The Issue: Presence of Particulate Matter: identified as glass

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

Class I — Serious Health HazardTerminated
Refund
October 2, 2023· Pfizer Inc.

Recalled Item: 4.2% Sodium Bicarbonate Injection

The Issue: Presence of Particulate Matter: identified as glass

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

Class I — Serious Health HazardTerminated
Refund
October 2, 2023· Pfizer Inc.

Recalled Item: 1% Lidocaine HCl Injection

The Issue: Presence of Particulate Matter: identified as glass

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

Class I — Serious Health HazardTerminated
Refund