fda_recall · device_recall · high

Medline Industries, LP — Class II recall: Medline Kits: 1) CATH LAB CDS, Model Number: CDS840228F; 2) IR PACK, Model Numb…

Event date
2026-04-29 00:00:00Z
Observed
2026-07-09 22:52:53Z
Source ID
Z-1835-2026
Payload hash
7d0d9981de35334ea45e4f2a

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The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.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