B. Braun Medical, Inc. recalls CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188
- Recall date
- July 10, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2472-2019
- FDA classification
- Class II
- Brand / firm
- B. Braun Medical, Inc.
- Sold / distributed
- CA FL MO TX MN AL GA NC IL PA
Why it was recalled
The filter capacity is not achieved due to damage of the filter membrane.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
CE18TKN ACCU-BLOC PERIFIX KIT NRFIT Catalog # 339188
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