Class II

Medical Device Recall: Medline CV ANESTHESIA - ROOM SET UP, REF DYNJ905503F; medical procedure convenience kit

MEDLINE INDUSTRIES, LP - Northfield · September 4, 2024

Reason for Recall

It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

15 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0152-2025

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.

MEDLINE INDUSTRIES, LP - Northfield Medical Device Recall: Medline CV ANESTHESIA - ROOM SET UP, REF DYNJ905503F; medical procedure convenience kit | SafeCheck