Class I

Medical Device Recall: Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q

Medline Industries, LP · August 21, 2025

Reason for Recall

The kits contain certain lots of cannula products where the catheter may not retain its shape.

Distribution

US Nationwide distribution in the state of CA.

States Affected

NATIONWIDE

Quantity Affected

828 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2670-2025

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.