Arrow International Inc recalls Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC;…
- Recall date
- October 17, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0647-2018
- FDA classification
- Class II
- Brand / firm
- Arrow International Inc
- Sold / distributed
- Distribution US Nationwide
Why it was recalled
These finished good kits may contain the incorrect Springwire Guide (SWG).
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018
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