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 9161–9180 of 17,529 recalls

April 5, 2018· Coastal Meds, LLC.

Recalled Item: ADENO-PLEX Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr.

The Issue: Presence of Particulate matter. Recall due to presence

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

Class II — Potential Health HazardTerminated
Refund
April 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr.

The Issue: Presence of Particulate matter. Recall due to presence

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

Class II — Potential Health HazardTerminated
Refund
April 5, 2018· Coastal Meds, LLC.

Recalled Item: METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr.

The Issue: Presence of Particulate matter. Recall due to presence

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

Class II — Potential Health HazardTerminated
Refund
April 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr.

The Issue: Presence of Particulate matter. Recall due to presence

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

Class II — Potential Health HazardTerminated
Refund
April 5, 2018· Coastal Meds, LLC.

Recalled Item: HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr.

The Issue: Presence of Particulate matter. Recall due to presence

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

Class II — Potential Health HazardTerminated
Refund
April 5, 2018· Coastal Meds, LLC.

Recalled Item: CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr.

The Issue: Presence of Particulate matter. Recall due to presence

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: Bendeka 25 mg/mL 4 mL MDVPF NDC 63459-0348-04 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: Otezla 30 mg tablet NDC 59572-0631-06 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: Altera Handset NDC 83490-0678-05 56 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 500 mg Tablet NDC 00378-2512-78 28 days supply and 21 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: Kalydeco 150 mg tablet blister

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: Cimzia 200 mg/mL PFS Kit #2 NDC 50474-0710-79 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: Sutent 50 mg capsules x28 NDC 00069-0550-38 42 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: Azithromycin 250 mg tablet #18 TEV NDC 50111-0787-66 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: Xolair 150 mg SDV NDC 50242-0040-62 28 days

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: Boost VHC Oral Liquid VAN #27 NDC 43900-0182-15 27 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: Bethkis 300 mg/4 mL Ampule #56 NDC 10122-0820-56 56 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: Dexamethasone 4 mg tablet NDC 49884-0087-01 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: Perjeta 420 mg/14 mL SDV Vials 50242-0145-01 21 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: Xtandi 40 mg capsule NDC 00469-0125-99 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