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IMPORTANT NOTICE PLEASE READ MARKET WITHDRAWAL VITAMIN C INJ. 100ml - LOT # 7020266 TEVA Animal Health is initiating a voluntary market withdrawal of Vitamin C Inj., with lot number 7020266. This market recall is based on the potential for particulate in the product. This recall is being made with the knowledge of the Food and Drug Administration. IMPORTANT NOTICE PLEASE READ MARKET WITHDRAWAL THIAMINE HCL INJ.- LOT # 7050818 TEVA Animal Health is initiating a voluntary market withdrawal of Thiamine 100 mg/ml bottles, with lot 7050818. This market recall is based on the potential for particulate in the product. This recall is being made with the knowledge of the Food and Drug Administration IMPORTANT NOTICE PLEASE READ MARKET WITHDRAWAL EPINEPHRINE INJ. 30ML - LOT # 8100753, LOT # 8110764, LOT # 7060857 TEVA Animal Health is initiating a voluntary market withdrawal of Epinephrine Inj. 30ml, with lot numbers 8100753, 8110764, 7060857. This market recall is based on the potential for particulate in the product. This recall is being made with the knowledge of the Food and Drug Administration. IMPORTANT NOTICE PLEASE READ MARKET WITHDRAWAL DURA-PEN 100ML AND 250ML AND PEN BP-48 500ML - B LACTAM CONTAINING PRODUCTS DURA-PEN, PRODUCT # 1-1111610 - 100ML WITH LOT # BL710136, BL710139, BL811162, BL811165, BL812176, BL901003. DURA-PEN, PRODUCT # 1-1111611 – 250ML WITH LOT # BL709118, BL710134, BL711144, BL711148, BL712151, BL712152, BL808128, BL809130, BL811164, BL901004, BL901013. PEN BP-48, PRODUCT # 1-1111613 – 500ML WITH LOT # BL 710121, BL711141, BL809129, BL811163, BL812177. TEVA Animal Health is initiating a voluntary market withdrawal of Dura-Pen and Pen BP-48, with lot numbers as listed above. While there is no data indicating the products do not meet finished product specifications throughout their shelf life, there is inconsistent or potentially incomplete documentation to support these products were developed, manufactured, controlled and tested in substantial compliance with Good Manufacturing Practices. This recall is being made with the knowledge of the Food and Drug Administration. |
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