FDA recall Z-1850-2026

Product

Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440

Reason for recall

The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

Distribution

US Nationwide distribution.

Key facts

Status

Ongoing

Initiation date

2026-02-25

Report date

2026-04-29

Voluntary/Mandated

Voluntary: Firm initiated

Location

Northfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1850-2026