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FDA (Device enforcement)Recalled 2024-10-16class ii

MEDLINE INDUSTRIES, LP - Northfield: MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZ

Hazard

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

Details from the source

Reason for recall: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position. Distribution: US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands Quantity: 3006 units Lot/code info: Codes: 1) PAIN1423A UDI-DI: 10193489201826 (each) 40193489201827 (case), Lot Numbers: 22GLA530, 23BLA921, 23DLA373, 23GLA522, 23ILA136, 23JLB217, 23KLA008; 2) PAIN1470A UDI-DI: 10193489957365 (each) 40193489957366 (case), Lot Numbers: 21JLA366, 21JLA956, 21LLA271, 22CLA831, 22DLA301, 22DLB149, 22FLA103; 3) PAIN1644 UDI-DI: 10193489331141 (each) 40193489331142 (case), Lot Numbers: 22FLA985, 23CLA104

UPC codes

10193489201826, 40193489201827, 10193489957365, 40193489957366, 10193489331141, 40193489331142

Source

Official record: FDA (Device enforcement)

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

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