Arrow International Inc recalls Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
- Recall date
- December 6, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0837-2020
- FDA classification
- Class II
- Brand / firm
- Arrow International Inc
- Sold / distributed
- US: FL
Why it was recalled
Potential sterility issue for specific lots of the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
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