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Drugs Recalls

17,897 recalls, newest first.

November 27, 2019DrugsFDA
Altaire Pharmaceuticals, Inc. recalls Perrigo Neomycin and Polymixin B Sulfates and Dexamethasone Ophthalmic Ointment, Net. Wt 3.5 gm, Sterile, Rx only, Manuf
Hazard: Lack of Assurance of Sterility
November 20, 2019DrugsFDA
KVK-Tech, Inc. recalls Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. b
Hazard: Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Male+, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC040
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Neuro, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC046
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0251
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Facial, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC01
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VS
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Relief +, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Immunexx, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Arthros, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-GI, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0211,
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Mesenchyme, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VS
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Lymph 1, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Prolo, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC055
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Collagen, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Infla, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC027
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Neuro 3, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Articula, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Systemic Detox, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Adipose, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Ithurts, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Ouch, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0500
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-MuSkel-Neural, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item:
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
8046255 Canada Inc. DBA Viatrexx recalls Viatrexx-Connectissue, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item:
Hazard: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
November 20, 2019DrugsFDA
Sato Pharmaceutical Inc. recalls Motion Sickness Strips (meclizine hydrochloride) 25 mg strips, 8-count box, Distributed by Sato Pharmaceutical INC. 2069
Hazard: Subpotent Drug
November 20, 2019DrugsFDA
Sato Pharmaceutical Inc. recalls WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets, packaged in a) 12 count (NDC 0363-1407-01, UPC 3 11917-18328 2 ) and
Hazard: Subpotent Drug
November 20, 2019DrugsFDA
Sato Pharmaceutical Inc. recalls Motion Sickness (meclizine hydrochloride) 25 mg tablets, 12-count box, Distributed by Sato Pharmaceutical INC. 20695 S.
Hazard: Subpotent Drug
November 20, 2019DrugsFDA
Sato Pharmaceutical Inc. recalls Zentrip (meclizine Hydrochloride), 25 mg strips, 8-strips per box, Distributed by Sato Pharmaceutical INC. 20695 S. West
Hazard: Subpotent Drug
November 20, 2019DrugsFDA
Amneal Pharmaceuticals, Inc. recalls Isotretinoin Capsules, USP 10 mg. Rx Only, 3 Prescription Blister Packs of 10- Capsules Each (30 Capsules)-. Distributed
Hazard: Failed Impurities/Degradation Specifications: Tretinoin levels slightly above specification limits.