FDA recall Z-1064-2023

MEDLINE INDUSTRIES, LP - Northfield · Class II · device

Product

UNIVERSAL CORE DR RUNNELS PACK. Sterile Procedural Tray

Reason for recall

Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Japan, Mexico, Panama, Turks & Caicos, United Arab Emirates.

Key facts

Status
Ongoing
Initiation date
2022-11-17
Report date
2023-02-15
Voluntary/Mandated
Voluntary: Firm initiated
Location
Northfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1064-2023