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 9141–9160 of 17,529 recalls

April 13, 2018· Boiron Inc.

Recalled Item: Calendula Cream

The Issue: Labeling: Labeling Error on Declared Strength; The outer

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

Class III — Low RiskTerminated
Refund
April 13, 2018· Septodont Inc.

Recalled Item: OraVerse (Phentolamine Mesylate) Injection

The Issue: Failed Impurities/Degradation: This recall has been initiated due

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

Class III — Low RiskTerminated
Refund
April 13, 2018· Lyne Laboratories, Inc.

Recalled Item: Fluocinolone Acetonide Topical Oil

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
April 13, 2018· Lyne Laboratories, Inc.

Recalled Item: Fluocinolone Acetonide Topical Oil

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
April 13, 2018· Lyne Laboratories, Inc.

Recalled Item: Fluocinolone Acetonide Topical Oil

The Issue: Subpotent Drug

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

Class II — Potential Health HazardTerminated
Refund
April 12, 2018· AMA Wholesale

Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack

The Issue: Undeclared Tadalafil

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

Class I — Serious Health HazardTerminated
Refund
April 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected

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

Class II — Potential Health HazardTerminated
Refund
April 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected

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

Class II — Potential Health HazardTerminated
Refund
April 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected

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

Class II — Potential Health HazardTerminated
Refund
April 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected

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

Class II — Potential Health HazardTerminated
Refund
April 10, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium TC-99M Mebrofenin

The Issue: Failed Stability Specifications

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

Class II — Potential Health HazardTerminated
Refund
April 10, 2018· Aidarex Pharmaceuticals LLC

Recalled Item: Ferrous Sulfate 325 MG tablet

The Issue: Presence of Foreign Tablets/Capsules

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

Class III — Low RiskTerminated
Refund
April 10, 2018· Pharmedium Services, LLC

Recalled Item: Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride

The Issue: cGMP deviations

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

Class III — Low RiskTerminated
Refund
April 9, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours

The Issue: Defective Delivery System: Out of specification for adhesive

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

Class II — Potential Health HazardTerminated
Refund
April 9, 2018· LEADIANT BIOSCIENCES, INC

Recalled Item: Cystaran (cysteamine ophthalmic solution) 0.44%

The Issue: Subpotent drug: Out of specification for an active

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

Class III — Low RiskTerminated
Refund
April 6, 2018· Sandoz Incorporated

Recalled Item: Triamterene and Hydrochlorothiazide Tablets

The Issue: Cross Contamination With Other Products: presence of unrelated

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

Class III — Low RiskTerminated
Refund
April 5, 2018· Coastal Meds, LLC.

Recalled Item: LIPO-B 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 PLUS 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-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: PYRIDOXINE 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