Class II

Medical Device Recall: Centurion Sterile Weitlaner Retractor, Reorder: 67315

MEDLINE INDUSTRIES, LP - Northfield · April 9, 2025

Reason for Recall

Three is the potential for the retractors to puncture through the sterile packaging.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

2100 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1765-2025

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.