Arrow International Inc recalls ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov…
- Recall date
- October 17, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0656-2018
- 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
ARROWg+ard Blue Plus Multi Lumen CVC (Central venous catheter); Product Code: AK-45703-ACDC; Exp. Dates Feb 2018 - Nov 2018
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