Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Vasostrict (vasopressin in 5% Dextrose) Injection Recalled by Par Sterile Products LLC Due to Superpotent Drug: Assay from the 3-month and 6-month...

Date: January 11, 2024
Company: Par Sterile Products LLC
Status: Ongoing
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Par Sterile Products LLC directly.

Affected Products

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

Quantity: 1721 cartons

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Par Sterile Products LLC

Par Sterile Products LLC has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report