Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx Only…
Reason Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.
411 recalls · Class II, newest first
Reason Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.
Reason CGMP Deviations: Potential Glass and Silicone particulates in product
Reason CGMP Deviations: Potential Glass and Silicone particulates in product
Reason CGMP Deviations: Potential Glass and Silicone particulates in product
Reason CGMP Deviations: Potential Glass and Silicone particulates in product
Reason CGMP Deviations: Potential Glass and Silicone particulates in product
Reason CGMP Deviations
Reason CGMP Deviations
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Reason Labeling: Incorrect or Missing Lot and/or Exp Date. The expiration date listed on the Repack Pouch Label is incorrect.
Reason Failed Impurities/Degradation Specification: Out of specification for organic impurities
Reason CGMP Deviations: products may not conform to the labeled specifications.
Reason CGMP Deviations: products may not conform to the labeled specifications.
Reason Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.
Reason Failed Dissolution Specifications