US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class II · Moderate risk Terminated

Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets

Reason Failed Impurities/Degradation Specifications: Kaitlib Fe Tablets has an out of specification result observed in long term stability study.

Lupin Pharmaceuticals Inc. NDC 68180-903-11 D-1565-2019
Class II · Moderate risk Completed

Clear Eyes Redness Relief

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. D-0490-2020
Class II · Moderate risk Completed

Clear Eyes Redness Relief

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. D-0489-2020
Class II · Moderate risk Completed

Clear Eyes Redness Relief

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. D-0487-2020
Class II · Moderate risk Completed

FreshKote Lubricant Eye Drops

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. NDC 15821-101-15 D-0483-2020
Class II · Moderate risk Completed

Puralube Ophthalmic Ointment

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. NDC 0574-4025-20 D-0474-2020
Class II · Moderate risk Completed

TRP Pink Eye Relief

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. NDC 17312-013-15 D-0471-2020
Class II · Moderate risk Completed

TRP Stye Relief

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. NDC 17312-014-13 D-0470-2020
Class II · Moderate risk Completed

TRP Blur Relief

Reason Lack of Assurance of Sterility

Altaire Pharmaceuticals, Inc. NDC 17312-002-11 D-0469-2020