Class II

Medical Device Recall: Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;

Covidien, LP · April 15, 2026

Reason for Recall

The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.

Distribution

Domestic: Nationwide distribution; International: Austria, Canada, Denmark, France, Italy;

States Affected

NATIONWIDE

Quantity Affected

2448 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2281-2026

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.