Delta Med SpA recalls WOLF-PAK Self Safe Safety IV Catheter: a) REF PIVD2010W b) REF PIV2210W c) REF PIV2475W
- Recall date
- June 21, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2305-2021
- FDA classification
- Class II
- Brand / firm
- Delta Med SpA
- Sold / distributed
- US Nationwide distribution in the states of FL and MN.
Why it was recalled
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
WOLF-PAK Self Safe Safety IV Catheter: a) REF PIVD2010W b) REF PIV2210W c) REF PIV2475W
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