Class II

Medical Device Recall: ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004C

MEDLINE INDUSTRIES, LP - Northfield · October 4, 2024

Reason for Recall

Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.

Distribution

US Nationwide distribution in the state of TN.

States Affected

NATIONWIDE

Quantity Affected

80 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0350-2025

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.