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 10661–10680 of 17,529 recalls

December 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Virt-Select Prenatal/Postnatal Softgels

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is

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

Class III — Low RiskTerminated
Refund
December 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Extra-Virt Plus DHA Prenatal/Postnatal Softgel

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is

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

Class III — Low RiskTerminated
Refund
December 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: Virt-Advance Prenatal/Postnatal Softgels

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is

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

Class III — Low RiskTerminated
Refund
December 12, 2016· VIRTUS PHARMACEUTICALS OPCO II L

Recalled Item: VirtPrex Prenatal/Postnatal Tablets

The Issue: cGMP Deviations: Active Pharmaceutical Ingredient (API) manufacturer is

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

Class III — Low RiskTerminated
Refund
December 9, 2016· Jersey Shore Supplements, LLC

Recalled Item: SLIMFIT X capsules

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
December 7, 2016· Novum Pharma, LLC

Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate

The Issue: Subpotent Drug: Out of specification result for pramoxine

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

Class III — Low RiskTerminated
Refund
December 6, 2016· Baxter Healthcare Corporation

Recalled Item: 10% Premasol sulfite-free (Amino Acid) Injection

The Issue: Discoloration: there were customer reports of yellow discolored

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

Class II — Potential Health HazardTerminated
Refund
December 6, 2016· Cipher Pharmaceuticals US LLC

Recalled Item: INOVA (benzoyl peroxide) 4%

The Issue: Subpotent Drug: Product label claim is 4% Benzoyl

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

Class III — Low RiskOngoing
Refund
December 6, 2016· Baxter Healthcare Corporation

Recalled Item: Fluconazole Injection

The Issue: Lack of Assurance of Sterility: confirmed customer complaints

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

Class II — Potential Health HazardTerminated
Refund
December 2, 2016· Ecolab, Inc.

Recalled Item: Endure 400 Scrub-Stat (chlorhexidine gluconate) Foam Forming Solution

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
December 2, 2016· Shire PLC

Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules

The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were

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

Class III — Low RiskTerminated
Refund
December 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Risedronate Sodium Delayed-release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 30, 2016· MS Bionic

Recalled Item: MegaJex Herbal Supplement

The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil

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

Class I — Serious Health HazardTerminated
Refund
November 23, 2016· Jeffreys Drug Store

Recalled Item: Domperidone capsules 10 mg

The Issue: Marketed without an approved NDA/ANDA for which safety

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

Class I — Serious Health HazardTerminated
Refund
November 22, 2016· Pfizer Inc.

Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection

The Issue: Subpotent Drug: Out of Specification (OOS) for potency

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

Class III — Low RiskTerminated
Refund
November 22, 2016· Les Emballages Knowlton Inc.

Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick

The Issue: Labeling: Label Mix Up- Incorrect back label applied

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

Class III — Low RiskTerminated
Refund
November 18, 2016· Raritan Pharmaceuticals, Inc.

Recalled Item: CVS pharmacy Kids' Ear Relief Oral Liquid 0.85 oz (25

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
November 18, 2016· Raritan Pharmaceuticals, Inc.

Recalled Item: CVS Health Homeopathic Infants Teething Tablets 135 count bottle Distributed

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
November 18, 2016· Raritan Pharmaceuticals, Inc.

Recalled Item: Kids' Relief Ear Relief Oral Liquid 0.85 fl oz. (25

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
November 18, 2016· Cantrell Drug Company

Recalled Item: Lidocaine HCl 1%

The Issue: Lack of Assurance of Sterility - the firm

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

Class II — Potential Health HazardTerminated
Refund