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: 40 cases (40 units) Lot/code info: Item Number: DYNJ901391D, Case UDI/GTIN: 40193489436595, Unit UDI/GTIN: 10193489436594, Lot Number: 22KBH254, 22IBI253
40193489436595, 10193489436594
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.