Arrow International Inc recalls Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. Th…
- Recall date
- August 8, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2741-2016
- FDA classification
- Class II
- Brand / firm
- Arrow International Inc
- Sold / distributed
- Nationwide Distribution to OH, IN, TN, NC, and KY.
Why it was recalled
Shipping carton labeling error.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.
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