FDA recall Z-1065-2023

MEDLINE INDUSTRIES, LP - Northfield · Class II · device

Product

FEMORAL ARTERY PACK-LF. 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-1065-2023