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FDA (Device enforcement)Recalled 2024-07-18class ii

Smiths Medical ASD Inc.: smiths medical portex, Thermovent 1200, 15mm/22mm: a) REF 100/582/000; b) REF 100/582/000JP; c) REF 100/582/000JS

Hazard

Uncertainty in the seal integrity of the sterile packaging.

Details from the source

Reason for recall: Uncertainty in the seal integrity of the sterile packaging. Distribution: Worldwide distribution. Quantity: 141,196 units Lot/code info: a) REF 100/582/000: UDI/DI 35019315022405, Lot Numbers: 4133230; UDI/DI 35019315010990, Lot Numbers: 4138707; UDI/DI 35019315011003, Lot Numbers: 4144947, 4147167; UDI/DI 35019315018156, Lot Numbers: 4135055, 4135056, 4135057, 4135059, 4135061, 4135063, 4147386, 4147387; UDI/DI 35019315022399, Lot Numbers: 4133228, 4133229; UDI/DI 35019315022429, Lot Numbers: 4141737, 4147168; UDI/DI 35019315022559, Lot Numbers: 4133814, 4147169; b) REF 100/582/000JP: UDI /DI 35019315018156, Lot Numbers: 4109285, 4109287, 4119729, 4131584, 4135055, 4135056, 4135057; c) REF 100/582/000JS: UDI/DI 35019315018156, Lot Numbers: 4135057

UPC codes

35019315022405, 35019315010990, 35019315011003, 35019315018156, 35019315022399, 35019315022429, 35019315022559

Source

Official record: FDA (Device enforcement)

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

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