Drug & medication recalls Moderate risk

Oxygen recalled over manufacturing violations

Recall date
December 19, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Roberts Home Medical LLC recalls Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home M…
Recall number
D-1002-2019
FDA classification
Class II
Brand / firm
Roberts Home Medical LLC
Sold / distributed
Product was distributed in MD, VA and the District of Columbia

Why it was recalled

CGMP Deviations

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

What was recalled

Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home Medical, Inc. Germantown, MD. 20875

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