Class II

Medical Device Recall: Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.

MEDLINE INDUSTRIES, LP - Northfield · October 15, 2024

Reason for Recall

Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.

Distribution

US Nationwide distribution in the states of AL, GA, MA, NJ, and PA.

States Affected

NATIONWIDE

Quantity Affected

48 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0534-2025

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.