Drug & medication recalls Moderate risk

RXQ Compounding LLC recalls Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Ath…

Recall date
June 19, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
D-1634-2019
FDA classification
Class II
Brand / firm
RXQ Compounding LLC
Sold / distributed
Nationwide USA

Why it was recalled

Crystallization

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Ascorbic Acid 500 MG/ML (Non-Corn) Injection (PFV), 50 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0173-10

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