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: 86 cases (152 units) Lot/code info: a. RHINOPLASTY PACK, Item Number: DYNJ27333F, Case UDI/GTIN: 40888277055293, Unit UDI/GTIN: 10888277055292, Lot Number: 22JMD960; b. OSC OTOLOGY PACK-LF, Item Number: DYNJ37384D, Case UDI/GTIN: 40193489306898, Unit UDI/GTIN: 10193489306897, Lot Number: 22HBY172; c. RHYZOTOMY, Item Number: DYNJ902288G, Case UDI/GTIN: 40193489885126, Unit UDI/GTIN: 10193489885125, Lot Number: 22JBU356,22JBT657;
40888277055293, 10888277055292, 40193489306898, 10193489306897, 40193489885126, 10193489885125
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.