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

MEDLINE INDUSTRIES, LP - Northfield: MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A

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: 3396 units Lot/code info: Codes: 1) DYNJRA9043S, UDI/DI 10193489888287(each) 40193489888288(case), Lot Numbers: 23CBE390, 23CBO216, 23EBM309, 23EBP979, 23EBS281, 23GBV099, 23HBG915, 23IBG610, 23IBG611, 23JBQ712, 23KBC341; 2) PAIN1622A, UDI/DI 10193489891690 (each) 40193489891691 (case), Lot Numbers: 21ELA821, 21GLA615, 21KLA308, 22ALA608, 22CLA681, 22ELB088, 22FLB075, 22GLA543, 22KLA019, 23BLA333, 23DLA466, 23HLA896

UPC codes

10193489888287, 40193489888288, 10193489891690, 40193489891691

Source

Official record: FDA (Device enforcement)

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

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