Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
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. Quantity: 15 cases (30 units) Lot/code info: Item Number: DYNJ0826625Q, Case UDI/GTIN: 40193489377942, Unit UDI/GTIN: 10193489377941, Lot Number: 22KMA163, 22JME722
40193489377942, 10193489377941
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.