Recalls / Class II
Class IID-0258-2024
Product
Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-0190-1
- Affected lot / code info
- Lot #: 20230921VAS-2, Exp. Date 03/19/2024
Why it was recalled
Subpotent Drug
Recalling firm
- Firm
- IntegraDose Compounding Services LLC
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 719 Kasota Ave Se, N/A, Minneapolis, Minnesota 55414-2842
Distribution
- Quantity
- 281 syringes
- Distribution pattern
- MN only
Timeline
- Recall initiated
- 2024-01-12
- FDA classified
- 2024-01-22
- Posted by FDA
- 2024-01-31
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0258-2024. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.