Delta Med SpA recalls NEO DELTA Self Safe, I.V. Catheter REF 3738222
- Recall date
- June 21, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2299-2021
- 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
NEO DELTA Self Safe, I.V. Catheter REF 3738222
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