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 17421–17440 of 17,529 recalls

May 8, 2012· Morton Salt Co.

Recalled Item: Morton

The Issue: Impurities/Degradation Products: The product was found to contain

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

Class III — Low RiskTerminated
Refund
May 8, 2012· Bayer HealthCare Pharmaceuticals Inc.

Recalled Item: Estradiol Hemihydrate M20 EP/USP Powder

The Issue: Cross Contamination w/Other Products: This active pharmaceutical ingredient

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

Class II — Potential Health HazardTerminated
Refund
May 7, 2012· Endo Pharmaceuticals, Inc.

Recalled Item: Endocet (oxycodone and acetaminophen) tablets

The Issue: Adulterated Presence of Foreign Tablets: Customer complaint that

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

Class III — Low RiskTerminated
Refund
May 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution

The Issue: Subpotent Drug: Salicylic acid is subpotent

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

Class III — Low RiskTerminated
Refund
May 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution

The Issue: Subpotent Drug: Salicylic acid is subpotent

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

Class III — Low RiskTerminated
Refund
May 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution

The Issue: Subpotent Drug: Salicylic acid is subpotent

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

Class III — Low RiskTerminated
Refund
May 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution

The Issue: Subpotent Drug: Salicylic acid is subpotent

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

Class III — Low RiskTerminated
Refund
May 7, 2012· Guthy-Renker LLC

Recalled Item: Rodan & Fields Proactiv Solution

The Issue: Subpotent Drug: Salicylic acid is subpotent

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

Class III — Low RiskTerminated
Refund
May 4, 2012· Linde Gas LLC

Recalled Item: LifeGas OXYGEN COMPRESSED UN1072 USP

The Issue: CGMP Deviations: The pressure gages, vacuum gages, and

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 1.5% Glycine Irrigation

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 0.45% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 5% Dextrose Injection USP

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 70% Dextrose Injection USP

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 20% Dextrose Injection

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 4, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation

The Issue: Lack of Assurance of Sterility: Hospira, Inc is

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

Class II — Potential Health HazardTerminated
Refund
May 2, 2012· Teva Pharmaceuticals USA, Inc.

Recalled Item: Zeosa (norethindrone and ethinyl estradiol tablets USP

The Issue: Impurities/Degradation: This recall is being carried out due

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

Class II — Potential Health HazardTerminated
Refund
May 1, 2012· Ben Venue Laboratories Inc

Recalled Item: Midazolam HCl Injection

The Issue: Short Fill: These products are being recalled because

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

Class II — Potential Health HazardTerminated
Refund