Class II

Medical Device Recall: Refer to RES

MEDLINE INDUSTRIES, LP - Northfield · March 3, 2025

Reason for Recall

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

States Affected

NATIONWIDE

Quantity Affected

28127 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1602-2025

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.