RecallRadar

FDA Drug recall D-0232-2024

Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose Vials per carton, Ready…

On 2024-01-24 the FDA classified a Class II recall of Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose Vials per carton, Ready… by Par Sterile Products, citing superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0232-2024
ClassificationClass II
Statusongoing
Initiated2024-01-11
Published2024-01-24
Last updated2026-09-13 11:52 UTC
CompanyPar Sterile Products
DistributionUS

Product

Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose Vials per carton, Ready to Use, For Intravenous Infusion, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977. NDC: 42023-237-10

Reason

Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

Identifiers

ndc42023-164-01
ndc42023-164-25
ndc42023-164-10
ndc42023-190-01
ndc42023-219-01
ndc42023-219-10
ndc42023-237-01
ndc42023-237-10
ndc42023-268-01
ndc42023-268-10
code_infoLot # 66702; Exp. 02/2025

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-0232-2024%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.