Class II

Medical Device Recall: O.R. SCISSORS, S/B, 5.5 STERILE, Medline Item No. DYND04000

MEDLINE INDUSTRIES, LP - Northfield · November 12, 2024

Reason for Recall

Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

21,440 total

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0755-2025

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.