Class II
Medical Device Recall: Medline Kits: 1) GENERAL LAPAROSCOPY, Model Number: CDS930027Y
Medline Industries, LP · February 25, 2026
Reason for Recall
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
75 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1840-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.