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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.

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Showing 6,821–6,840 of 17,964 drug recalls

Drug Recall Completed Historical recordClass II

CVS Health Preservative Free Lubricant Gel Drops Dry Eye Relief, Item#: 634634, Product Size: 0.6 mL x 30, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895

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 Lubricant Gel Drops Multi Dose Preservative Free, 7.5 mL, NDC 49035-882-52

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 Ophthalmic Ointment, 3.5 gram, Mfd. for Perrigo, Minneapolis, MN 55427, NDC 0574-4025-20

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 Petrolatum Ophthalmic Ointment, Net Wt 3.5 gram (1/8 oz), Mfd. for Perrigo, Minneapolis, MN 55427, NDC 0574-4025-35

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

Nano Tears MXP Forte Clear Emollient Lubricant Gel Drops Twin Pack, Product Size: 2 x 10 mL, NDC 59390-144-51

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

TRP Pink Eye Relief, 10 mL, NDC 17312-013-15

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

TRP Stye Relief, 4 g, NDC 17312-014-13

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

TRP Blur Relief, 15 mL, NDC 17312-002-11

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

TRP/ TARGET up & up intensive relief lubricating eye drop, 10 mL

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

Natural Ophthalmics Allergy Desensitization Eye Drops, 15 mL, NDC 68770-120-15

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

Natural Ophthalmics Cataract Eye Drops with Cineraria, 15 mL, 25 mL, NDC 68770-130-15

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

Natural Ophthalmics Tear Stimulation Forte Dry Eye Drops, 15 mL, NDC 68770-104-15

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

Natural Ophthalmics Ortho-K Thin Eye Drops, 15 mL, NDC 68770-144-15

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

Natural Ophthalmics Women's Tear Stimulation Dry Eye Drops, 15 mL, NDC 68770-103-15

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

Natural Ophthalmics Ortho-K Thick Comfort Gel, 15 mL, NDC 68770-143-15

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

Altaire Diclofenac Sodium Opthalmic Solution, 0.1%, 5 mL, Rx only, Manufactured Altaire Pharmaceuticals, NDC 59390-149-05

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

Grandall Colirio Ojo De Aguila Eye Drops, Sterile, Net Wt 1/2 fl oz (15 mL) Dist. By Grandall Distributing Co.Inc., Glendale, CA 91204-2707

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

Accutome Rx Accu-WASH, 4 FL OZ (118 mL), Manufactured for Accutome Inc 3222 Phoenixville Pike Malvern, PA 19355 USA Mfd. By: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931, NDC 63448-411-04

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

Accutome Rx Accu-WASH, 4 FL OZ (118 mL), Manufactured for: Accutome Inc 3222 Phoenixville Pike Malvern, PA 19355 USA, Mfd. By: Altaire Pharmaceuticals, Inc. Aquebogue, NY 11931, NDC 63448-411-04

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

CVS Health Lubricating Gel Drops for Anytime Use, Item#: 563420, Product Size: 10 mL, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895

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 →

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.