FDA recall Z-2670-2025

Medline Industries, LP · Class I · device

Product

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

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.

Key facts

Status
Ongoing
Initiation date
2025-08-21
Report date
2025-10-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Northfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2670-2025