Praxair product recalled over manufacturing violations
- Recall date
- September 16, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Praxair Inc. recalls UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-…
- Recall number
- D-0782-2016
- FDA classification
- Class III
- Brand / firm
- Praxair Inc.
- Sold / distributed
- Nationwide
Why it was recalled
CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
UN1002 Air, Compressed, Breathing Grade, USP, Distributed by Praxair Distribution, Inc. Roseville, MN 55113, NDC 59579-006.
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