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 9221–9240 of 17,529 recalls

April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Temozolomide 250 mg NDC 43975-0257-05 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Ondansetron 8 mg tablet NDC 57237-0076-30 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Promacta 50 mg tablet NDC 00078-0686-15 30 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Revlimid 25 mg oral cap NDC 59572-0425-21 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Enbrel PFS 50 mg/mL Inj #4 NDC 58406-0435-04 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Praluent 75 mg Pen (2 pens/Pkg) NDC 00024-5901-02 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Revlimid 5 mg oral cap NDC 59572-0405-28 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Capecitabine 150 mg Tablet NDC 00378-2511-91 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Letrozole 2.5 mg tab NDC 51991-0759-33 30 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Xalkori 250 mg cap NDC 00069-8140-20 30 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Tecfidera 240 mg capsule NDC 64406-0006-02 30 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Temozolomide 20 mg NDC 43975-0253-05 28 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 3, 2018· Kroger Specialty Pharmacy, Inc.

Recalled Item: Pediasure Liq. Vanilla G+G (CAN) #24 24 days supply

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardTerminated
Refund
April 2, 2018· Diamond Wipes International, Inc.

Recalled Item: WipeEssentials Wet Wipes (benzalkonium chloride 0.13%)

The Issue: CGMP Deviations: finished products were manufactured with poor

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

Class II — Potential Health HazardTerminated
Refund
April 2, 2018· Diamond Wipes International, Inc.

Recalled Item: ACURE

The Issue: CGMP Deviations: finished products were manufactured with poor

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

Class II — Potential Health HazardTerminated
Refund
March 30, 2018· AVKARE Inc.

Recalled Item: Amantadine HCl Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 30, 2018· Marcas Usa Llc

Recalled Item: PASTA DE LASSAR ANDROMACO Skin Protection

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardTerminated
Refund
March 29, 2018· United Pacific Co Ltd

Recalled Item: Zhong Hua Jiu (menthol 1%) Patch

The Issue: CGMP Deviations: the product was produced with substandard

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

Class II — Potential Health HazardTerminated
Refund
March 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology

The Issue: Subpotent Drug: Product crystallization with accompanying low out

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

Class III — Low RiskTerminated
Refund
March 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology

The Issue: Subpotent Drug: Product crystallization with accompanying low out

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

Class III — Low RiskTerminated
Refund