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 14141–14160 of 17,529 recalls

November 14, 2014· Attix Pharmaceuticals

Recalled Item: Doxapram HCI Monohydrate active pharmaceutical ingredient packaged in...

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 14, 2014· Attix Pharmaceuticals

Recalled Item: Losartan Potassium active pharmaceutical ingredient packaged in varying grams or

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 14, 2014· Attix Pharmaceuticals

Recalled Item: Cantharidin active pharmaceutical ingredient packaged in varying grams or kg

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 14, 2014· Attix Pharmaceuticals

Recalled Item: Levosulpiride active pharmaceutical ingredient packaged in varying grams or kg

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 14, 2014· Attix Pharmaceuticals

Recalled Item: Aminocaproic Acid active pharmaceutical ingredient packaged in varying grams or

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 14, 2014· Attix Pharmaceuticals

Recalled Item: Cyclophosphamide Monohydrate active pharmaceutical ingredient packaged in...

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 14, 2014· Attix Pharmaceuticals

Recalled Item: Ketoconazole active pharmaceutical ingredient packaged in varying grams or kg

The Issue: Penicillin Cross Contamination: All lots of all products

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

Class II — Potential Health HazardTerminated
Refund
November 12, 2014· Fresenius Kabi USA, LLC

Recalled Item: GENTAMICIN INJECTION

The Issue: Defective Container: Vials may be missing stoppers

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

Class II — Potential Health HazardTerminated
Refund
November 10, 2014· Reckitt Benckiser LLC

Recalled Item: Mucinex DM (guaifenesin 600mg and dextromethorphan HBr 30mg)

The Issue: Defective container: A customer complaint revealed the presence

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

Class III — Low RiskTerminated
Refund
November 10, 2014· Baxter Healthcare Corp.

Recalled Item: Potassium Chloride Injection

The Issue: Labeling: Label Error On Declared Strength: Bags of

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: HCG Low Dose 30 IU/0.1 mL

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Tri-Mix (PGE-10MCG/PAP-30MG/PT 5Ml vials

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: HCG 10

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Tri Mix PF SYR 0.5 mL Inj.

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: HCG Low Dose 10 IU / 0.1 mL

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Phenylephrine HCl (100 mcg/mL syr) in 0.9% NaCl 1 mg / 10 mL

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: HCG 200 IU/mL Injection

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Leuprolide 50 mcg/0.1 mL Micro Lupron Kit

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Methyl B12 25 mg/mL Inj.

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: HCG-20

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund