Class II

Medical Device Recall: MEDLINE KIT CV I II, REF DYNJ906071B

MEDLINE INDUSTRIES, LP - Northfield · August 28, 2024

Reason for Recall

Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

56 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0123-2025

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 KIT CV I II, REF DYNJ906071B | SafeCheck