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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