Class II

Medical Device Recall: Medline procedural kits labeled as: CIRCUMCISION TRAY, Pack Number DYNDA2271

MEDLINE INDUSTRIES, LP - Northfield · April 8, 2024

Reason for Recall

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Distribution

Worldwide

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2749-2024

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.

MEDLINE INDUSTRIES, LP - Northfield Medical Device Recall: Medline procedural kits labeled as: CIRCUMCISION TRAY, Pack Number DYNDA2271 | SafeCheck