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Medicine / D-0876-2026

U.S. Food and Drug AdministrationD-0876-2026

Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05

Class II Distributed nationwide or U.S.-wide Status: Ongoing

What was recalled

Buprenorphine Hydrochloride, Injection 0.3 mg/mL, Rx Only, 5 x 1 mL Single Dose Vials, Manufactured for: Endo USA, Malvern, PA, NDC 42023-179-05

Recalling firm

Par Health USA, LLC

Reason for recall

Crystallization

Where it went

U.S. Nationwide

Shown as U.S. Food and Drug Administration published it (shortened where marked …). Recall Shelf does not change recall facts and is not affiliated with the agency.