Class II

Medical Device Recall: Sterile CoFlex NL: Latex Free Flexible Cohesive Bandage, Tan, 4INx5YD (5400S)

Andover Healthcare Inc. · April 2, 2024

Reason for Recall

A packaging seal gap could impact the sterility of the product.

Distribution

US Nationwide distribution in the states of CA, CO, GA, IA, IN, OH, MN, NC, PA, TX, VA, WA.

States Affected

NATIONWIDE

Quantity Affected

108 cases (1,944 individual product packages)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1828-2024

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.