fda_recall · device_recall · high

Medline Industries, LP — Class II recall: Medline Kits: 1) BWNBORO CRANIOTOMY PACK-LF, Model Number: DYNJ32841F; 2) CRA…

Event date
2026-04-29 00:00:00Z
Observed
2026-07-09 22:52:59Z
Source ID
Z-1849-2026
Payload hash
7760623a23a1189409546d24

Summary

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Status: Ongoing.

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