fda_recall · device_recall · high

ARROW INTERNATIONAL, LLC — Class II recall: Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 F…

Event date
2026-04-29 00:00:00Z
Observed
2026-07-09 22:53:01Z
Source ID
Z-1917-2026
Payload hash
028e366dfaf96ed64797cb69

Summary

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured Status: Ongoing.

Informational only. Not legal, financial, or medical advice.