Nipro Medical Corporation recalls NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch. Item code FS+173230BC.
- Recall date
- April 1, 2014
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0599-2016
- FDA classification
- Class III
- Brand / firm
- Nipro Medical Corporation
- Sold / distributed
- US distribution including TN.
Why it was recalled
Device has the potential to have torn wings.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
NIPRO SafeTouch II Safety AVF Needle, 17G x 1 ¿ inch. Item code FS+173230BC.
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