fda_recall · device_recall · high

Medline Industries, LP — Class II recall: Medline Kits: 1) ARTHROGRAM TRAY, Model Number: DYNJ07425; 2) TOL NEURO ANGIO…

Event date
2026-04-29 00:00:00Z
Observed
2026-07-09 22:53:02Z
Source ID
Z-1844-2026
Payload hash
f7f2c2c8ab11cabce4cdfb93

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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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