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

MEDLINE INDUSTRIES, LP - Northfield: UNIVERSAL CORE DR RUNNELS PACK. Sterile Procedural Tray

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: 20 cases (120 units) Lot/code info: Item Number: DYNJ52230, Case UDI/GTIN: 40889942252269, Unit UDI/GTIN: 10889942252268, Lot Number: 22IBJ862

UPC codes

40889942252269, 10889942252268

Source

Official record: FDA (Device enforcement)

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

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