The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
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
10193489888287, 40193489888288, 10193489891690, 40193489891691
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.