Reason: Lack of Assurance of Sterility
Distributed: Nationwide in the USAReason: Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some Gabapentin tablets 800 mg comingled in Gabapentin 600 mg 500 count bottles.
Distributed: Nationwide in the USA and Puerto RicoReason: Sub-Potent Drug: Out of specification for assay at the 24 month interval.
Distributed: Nationwide and Puerto Rico.Reason: Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Distributed: Product was distributed nationwide in the United States and Puerto Rico, and to Australia, China, Canada, Columbia, Mexico, Brazil, Malaysia, Chile, Dominic Republic, Singapore, Thailand, Ireland, Germany, South Korea, Argentina, Pakistan, Oman, IndiaReason: Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Distributed: Product was distributed nationwide in the United States and Puerto Rico, and to Australia, China, Canada, Columbia, Mexico, Brazil, Malaysia, Chile, Dominic Republic, Singapore, Thailand, Ireland, Germany, South Korea, Argentina, Pakistan, Oman, IndiaReason: Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Distributed: Product was distributed nationwide in the United States and Puerto Rico, and to Australia, China, Canada, Columbia, Mexico, Brazil, Malaysia, Chile, Dominic Republic, Singapore, Thailand, Ireland, Germany, South Korea, Argentina, Pakistan, Oman, IndiaReason: Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Distributed: Product was distributed nationwide in the United States and Puerto Rico, and to Australia, China, Canada, Columbia, Mexico, Brazil, Malaysia, Chile, Dominic Republic, Singapore, Thailand, Ireland, Germany, South Korea, Argentina, Pakistan, Oman, IndiaReason: Failed Impurities/Degradation Specifications
Distributed: Product was distributed to 16 distributors and 8 wholesalers who may have further distributed the product nationwide.Reason: Lack of sterility assurance: Recall of certain batches of 0.9% Sodium Chloride for Injection USP in EXCEL¿ Plus IV Container product due to the possibility of an incomplete seal that may cause leakage. The impacted lots may exhibit microscopic channel leaks near the port assembly of the product.
Distributed: USA Nationwide.Reason: Lack of sterility assurance: Recall of certain batches of 0.9% Sodium Chloride for Injection USP in EXCEL¿ Plus IV Container product due to the possibility of an incomplete seal that may cause leakage. The impacted lots may exhibit microscopic channel leaks near the port assembly of the product.
Distributed: USA Nationwide.