Skip to main content
Get Alerts

FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

Filters
Recall details
Location
Date range
Clear filters

Showing 6,921–6,940 of 17,964 drug recalls

Drug Recall Completed Historical recordClass II

Equate Support Advanced Lubricating Eye Drops, Preservative Free, Sterile, 25 Single-Use Containers, 0.02 Fl. oz. (0.6 mL), W-M item #: 563031654, Distributed by: Walmart Inc., Bentonville, AR 72716, NDC 49035-882-54

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Equate Support Advanced Twin Pack W-M item #: 567371433, Package Size: 2 x 15 mL, Distributed by: Wal-Mart Stores Inc., Bentonville, AR 72716, NDC 49035-885-49

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Equate Night & Day Restore Tears Lubricant Eye Pack W-M item #: 567368000, Package Size: 3.5g and 15mL, Distributed by: Wal-Mart Stores Inc., Bentonville, AR 72716, NDC 49035-883-59

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Equate Restore PM Nighttime Lubricant Eye Ointment, Sterile, Net Wt. 0.125 oz. (3.5g), Distributed by: Walmart Stores Inc., Bentonville, AR 72716, W-M item #551282425, NDC 49035-191-50

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Equate Comfort Gel Lubricant Eye Gel Twin Pack W-M item #: 552374319, Package Size: 2 x 15 mL, Distributed by: Walmart Inc., Bentonville, AR 72716, NDC 49035-197-49

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Equate Sterile Lubricant Stye Ointment, Net wt. 0.125 oz. (3.5g), Distributed by: Wal-Mart Stores Inc., Bentonville, AR 72716, NDC 49035-875-50

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Equate Restore Tears Lubricant Eye Drops Twin Pack W-M item #: 552374320, Package Size: 2 x 15 mL, Distributed by: Walmart Inc., Bentonville, AR 72716, NDC 49035-189-49

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Walgreen's Lubricant Eye Ointment, Mineral Oil 42.5%/White Petrolatum 57.3% /Eye Lubricant, Net Wt. 0.125 oz. (3.5g), Distributed by: Walgreen Co., 200 Wilmot Rd, Deerfield, IL 60015, Item #801486, NDC 0363-0191-50

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Walgreens Sodium Chloride Ophthalmic Solution, 5% Hypertonicity Eye Drops, 0.5 oz (15 mL), Distributed by : Walgreen Co 200 Wilmot Road Deerfield IL 60015 NDC 0363-0193-13

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Walgreens Sodium Chloride Ophthalmic Ointment, 5% Hypertonicity Eye Ointment Sterile, Net Wt. 0.125 oz (3.5 g), Distributed by Walgreen Co. 200 Wilmot Road Deerfield, IL 60015, NDC 0363-7500-50

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Lubricant Eye Drops Moisturizing Twin Pack Walgreens item #: 801477, Package Size: 2 x 15 mL, NDC 0363-0185-49

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Lubricant Eye Drops Moisturizing (Carboxymethycellulose Sodium 0.5% Eye Lubricant), 0.5 oz. (15 mL), Distributed by: Walgreens Co., 200 Wilmot Road, Deerfield, IL 60015, Item #801483

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Puralube Ointment Petrolatum Ophthalmic Ointment, Sterile Ocular Lubricant, Net Wt. 1 g (NDC 0574-4025-11) and Net Wt. 3.5 g (1/8 oz.) (NDC 0574-4025-35), Manufactured for Perrigo, Minneapolis, MN 55427

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Perrigo Sulfacetamide Sodium Ophthalmic Ointment USP, 10% Sterile, Rx only, Net Wt 3.5 g, Manufactured For: Perrigo Minneapolis, MN 55427, NDC 0574-4190-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Perrigo Bacitracin Ophthalmic Ointment, Net Wt. 3.5 g (1/8 oz), Rx only, Manufactured For: Perrigo Minneapolis, MN 55427, NDC 0574-4022-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Polycin (bacitracin zinc and polymyxin B sulfate) Ophthalmic Ointment USP, Net. Wt. 3.5 g (1/8 oz.), Rx only, Manufactured for Perrigo, Minneapolis, MN 55427, NDC 0574-4021-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Perrigo Sterile Neo-Polycin HC (neomycin and polymixin B sulfates, bacitracin zinc and hydrocortisone acetate) Ophthalmic Ointment USP, Net Wt. 3.5 g (1/8 oz), Rx only, Mfd. For Perrigo Minneapolis, MN 55427, NDC 0574-4144-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Completed Historical recordClass II

Perrigo Neo-Polycin neomycin and polymixin B sulfates and bacitracin zinc Ophthalmic Ointment Net Wt. 3.5 g, Rx only, Manufactured for Perrigo Minneapolis, MN 55427 NDC 0574-4250-35

by Altaire Pharmaceuticals, Inc.

Reason
Lack of Assurance of Sterility
Recall initiated
July 2, 2019
Reported by FDA
November 27, 2019
Distribution
U.S.A. Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. by: KVK-Tech, Inc. Newtown PA 18940; NDC 10702-150-16

by KVK-Tech, Inc.

Reason
Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
Recall initiated
November 1, 2019
Reported by FDA
November 20, 2019
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0025, NDC 73069-039-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason
Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Recall initiated
October 15, 2019
Reported by FDA
November 20, 2019
Distribution
Distributed to physicians Nationwide throughout the United States and Puerto Rico.

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.