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 16401–16420 of 17,529 recalls

May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: HCG 11000u w/B-12

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Minoxidil 10% 60ml

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Double Strength PGE1 40mcg/ml

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Lipotropic 1.5ml PFS

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Depo-Testadiiol

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Mic Ultra-Sulfur Free 30ml

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Betamethasone 6mg PF 10ml

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 28, 2013· Main Street Family Pharmacy, LLC

Recalled Item: Tri-Mix SS Pap 30mg

The Issue: The firm received seven reports of adverse reactions

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

Class II — Potential Health HazardTerminated
Refund
May 27, 2013· Earthlabs, Inc. DBA Wise Woman Herbals

Recalled Item: Eyebright Concentrate Topical Eye Rinse

The Issue: Lack of Assurance of Sterility; Lack of Assurance

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

Class II — Potential Health HazardTerminated
Refund
May 25, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion

The Issue: Presence of Particulate Matter; single visible particulate was

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

Class II — Potential Health HazardTerminated
Refund
May 25, 2013· Fresenius Kabi USA, LLC

Recalled Item: Magnesium Sulfate Injection

The Issue: Presence of Particulate Matter: Glass particulate matter was

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

Class I — Serious Health HazardTerminated
Refund
May 23, 2013· Indelicare LLC

Recalled Item: INK-EEZE Tattoo Numbing Spray

The Issue: Marketed without an approved NDA/ANDA: INK-EEZE Tattoo Numbing

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

Class II — Potential Health HazardTerminated
Refund
May 23, 2013· Indelicare LLC

Recalled Item: INK-EEZE Tattoo Black Label Numbing Spray

The Issue: Marketed without an approved NDA/ANDA: INK-EEZE Tattoo Numbing

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Fresenius Kabi USA, LLC

Recalled Item: Folic Acid Injection

The Issue: Failed Impurities/Degradation Specification

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

Class III — Low RiskTerminated
Refund
May 21, 2013· American Health Packaging

Recalled Item: Zolpidem Tartrate Tablets 5 mg

The Issue: Unit Dose Mispackaging: This recall event is due

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Baxter Healthcare Corp.

Recalled Item: Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Specific lot numbers

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Baxter Healthcare Corp.

Recalled Item: Lidocaine Hydrochloride and 5% Dextrose Injection

The Issue: Lack of Assurance of Sterilty: Specific lot numbers

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Sun Pharmaceutical Industries Inc.

Recalled Item: Nimodipine Capsules 30 mg

The Issue: Crystallization; crystallized nimodipine

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection

The Issue: Lack of Assurance of Sterility: Specific lot numbers

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Baxter Healthcare Corp.

Recalled Item: Metronidazole Injection USP

The Issue: Lack of Assurance of Sterility: Specific lot numbers

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

Class II — Potential Health HazardTerminated
Refund