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FDA (Device enforcement)Recalled 2024-07-24class ii

Cardinal Health 200, LLC: (a) CardinalHealth Salem Sump Dual Lumen Stomach Tube, 12 Fr/Ch (4.0 mm) x 48 in. (122 cm), Model #8888264929, Sterile; (b) CardinalHealth Salem Sump Dual Lumen Stomach Tube,

Hazard

The firm received reports of breakage in the Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made.

Details from the source

Reason for recall: The firm received reports of breakage in the Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made. Distribution: Distribution was nationwide, including Puerto Rico and Guam. There was also government/military distribution. Foreign distribution was made to Chile. Quantity: 24,761,100 tubes total Lot/code info: All lot numbers. UDI-DI numbers: (a) 8888264929, UDI-DI 10192253012477; (b) 8888264945, UDI-DI 10192253012491; (c) 8888264960, UDI-DI 10192253012514; and (d) 8888264986, UDI-DI 10192253012538;

UPC codes

10192253012477, 10192253012491, 10192253012514, 10192253012538

Source

Official record: FDA (Device enforcement)

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

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