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Provepharm Inc. recalls Dihydroergotamine Mesylate Injection, solution for injection, USP, 1 mg/mL Ampules, Rx Only, Distributed by: Provepharm

Recalled December 25, 2024 · FDA recall D-0150-2025 · Provepharm

Hazard
Discoloration · FDA Class II
Units
2160 packs/5 ampules per pack = 10,800 ampules
Sold at
Nationwide within the United States

Description

Discoloration

Product
Dihydroergotamine Mesylate Injection, solution for injection, USP, 1 mg/mL Ampules, Rx Only, Distributed by: Provepharm Inc. 100 Springhouse Drive Suite 105, Collegeville, PA 19426, NDC 81284-411-05
Manufacturer(s)
Provepharm Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Provepharm Inc. recalls Dihydroergotamine Mesylate Injection, solution for injection, USP, 1 mg/mL Ampules, Rx Only, Distributed by: Provepharm | RecallWatchUSA