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 6301–6320 of 17,529 recalls

November 1, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP

The Issue: Presence of Foreign substance: identified as a dead

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

Class III — Low RiskTerminated
Refund
November 1, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cephalexin for Oral Suspension USP

The Issue: Presence of Foreign substance: identified as a dead

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

Class III — Low RiskTerminated
Refund
October 31, 2019· Fagron, Inc

Recalled Item: LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL)

The Issue: Microbial contamination of non-sterile product

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

Class II — Potential Health HazardTerminated
Refund
October 30, 2019· Avantor Performance Materials Inc

Recalled Item: Potassium Phosphate

The Issue: Failed Stability Specifications: Product exceeds compendia and firm's

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

Class II — Potential Health HazardTerminated
Refund
October 28, 2019· Lannett Company, Inc.

Recalled Item: Lannett Ranitidine Syrup (Ranitidine Oral Solution

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
October 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
October 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
October 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
October 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

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

Class II — Potential Health HazardTerminated
Refund
October 25, 2019· ICU Medical Inc

Recalled Item: 0.9% SODIUM CHLORIDE INJECTION

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardTerminated
Refund
October 25, 2019· ICU Medical Inc

Recalled Item: LACTATED RINGER'S Injection

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund
October 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine

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

Class II — Potential Health HazardTerminated
Refund