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Catheter Repair Kit

FDA product code PWR · Class 2 · General Hospital

3
Registered devices
29
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

ARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATEDARROW — TELEFLEX INCORPORATED

Recent recalls

DateFirmReason
2026-04-21ARROW INTERNATIONAL, LLCLidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.