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FDA (Device enforcement)Recalled 2022-11-17class ii

MEDLINE INDUSTRIES, LP - Northfield: Sterile Procedural Trays, labeled as the following: GENERAL ENDOSCOPY

Hazard

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

Details from the source

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: 48 cases (96 units) Lot/code info: Item Number: DYNJ903826D, Case UDI/GTIN: 40195327177790, Unit UDI/GTIN: 10195327177799, Lot Number: 22IBR004;

UPC codes

40195327177790, 10195327177799

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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