Centurion Medical Products Corporation recalls PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
- Recall date
- July 15, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0256-2020
- FDA classification
- Class II
- Brand / firm
- Centurion Medical Products Corporation
- Sold / distributed
- IL
Why it was recalled
Supplier initiated recall of the GRIPPER Needles
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
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