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 7241–7260 of 17,529 recalls

June 12, 2019· Infusion Options, Inc.

Recalled Item: DARZALEX 1008 MG / 500 ML NS IVPB

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
June 12, 2019· Infusion Options, Inc.

Recalled Item: Oxytocin 60 units/1000 mL Lactated Ringers Intravenous Solution

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
June 12, 2019· Infusion Options, Inc.

Recalled Item: CARBOPLATIN 174 MG / 250ml NS IVPB

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
June 12, 2019· Infusion Options, Inc.

Recalled Item: Fluorouracil 560 MG / 11.2 ML IVP

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
June 12, 2019· Infusion Options, Inc.

Recalled Item: DECITABINE 40 MG / 100 ml NS IVPB

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
June 12, 2019· Infusion Options, Inc.

Recalled Item: PEMBROLIZUMAB 200 MG / 100 ML NS IVPB

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
June 12, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Topical Solution 30mg of testosterone per pump actuation *

The Issue: Defective Container; actuator may improperly function and affect

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

Class III — Low RiskTerminated
Refund
June 10, 2019· Preferred Pharmaceuticals, Inc

Recalled Item: Robafen DM

The Issue: CGMP Deviations: Potential product contamination with Burkholderia cepacia

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

Class II — Potential Health HazardTerminated
Refund
June 7, 2019· PharMEDium Services, LLC

Recalled Item: Hydromorphone HCl in 0.9% sodium chloride

The Issue: Incorrect Product Formulation; Firm's customer resource center (CRC)

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

Class I — Serious Health HazardTerminated
Refund
June 7, 2019· Akorn Inc

Recalled Item: Myorisan (isotretinoin capsules

The Issue: Labeling: Label mix-up: Product secondary carton erroneously states

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

Class III — Low RiskTerminated
Refund
June 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 50 mg TABLET BULK 90 count bottles and 1000 count bottles

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) dete

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

Class II — Potential Health HazardOngoing
Refund
June 6, 2019· Teva Pharmaceuticals USA

Recalled Item: LOSARTAN POTASSIUM 100 mg TABLET BULK 90 count bottles

The Issue: CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) dete

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

Class II — Potential Health HazardOngoing
Refund
June 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL

The Issue: cGMP Deviations: Firm was notified by their supplier

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine HCL Oral Solution 1 mg/mL

The Issue: cGMP Deviations: Firm was notified by their supplier

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2019· P & L Developments, LLC

Recalled Item: Cetirizine Oral Solution 1 mg/mL

The Issue: cGMP Deviations: Firm was notified by their supplier

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Allergy Relief D

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation

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

Class II — Potential Health HazardTerminated
Refund
June 5, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Wal-Fex D Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg/

The Issue: Testing of Fexofenadine HCl and Pseudoephedrine Failed Impurities/Degradation

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

Class II — Potential Health HazardTerminated
Refund
June 3, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Estradiol Vaginal Inserts USP 10 mcg

The Issue: Defective Delivery System: Estradiol Vaginal Inserts USP plunger

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

Class II — Potential Health HazardTerminated
Refund