Recalling firm
American Regent, Inc.
Product type
Drug
Status
Terminated
Report date
2024-05-29
Distribution
USA Nationwide
Firm state
OH
Product quantity
2,352 vials
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Validation & QualificationReason for recall
Subpotent product in addition to having out-of-specification results for impurities.
Product description
Vasopressin Injection, USP, 200 Units per 10 mL (20 Units per mL), 10 mL Multiple-Dose Vial, Rx only, For Intravenous Infusion, American Regent, Inc., Shirley, NY 11967, NDC 0517-1030-01
Code / lot info
Lot #: 23061L1C0, Exp 1/31/2025
Other recalls SPEQ maps to Validation & Qualification
See all Validation & Qualification recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.