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Catheter Guide Wire Kit

FDA product code OFB · Class 2 · Cardiovascular

2
Registered devices
48
Adverse events
2
Recalls
0
510(k) clearances

Devices with this code

Vascular Kit — ARGON MEDICAL DEVICES, INC.ARROW — 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
2026-03-11ARROW INTERNATIONAL, LLCDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

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