RecallRadar

FDA Drug recall D-0325-2024

Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx Only, 719 Kasota…

On 2024-02-21 the FDA classified a Class II recall of Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx Only, 719 Kasota… by Integradose Compounding Services, citing sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0325-2024
ClassificationClass II
Statusongoing
Initiated2024-01-22
Published2024-02-21
Last updated2026-09-13 11:52 UTC
CompanyIntegradose Compounding Services
DistributionMN

Product

Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN, Compounded Drug Not for Resale. Office Use Only, NDC 71139-0190-1.

Reason

Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.

Identifiers

code_infoLot #s: 20230929VAS-2, Exp. 02/29/2024; 20231004VAS-2, Exp. 04/01/2024; Lot 20231010VAS-2,Exp. 04/07/2024; Lot 20231013VAS-2, Exp. 04/10/2024

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0325-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.