Product Safety Recalls

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TELEFLEX LLC Recall 92373

Description: RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030

TELEFLEX LLC Recall 92373 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1896-2023
Event ID92373
Event DescriptionRUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480030
Product TypeDevices
DistributionUS Nationwide distribution including Puerto Rico.
Quantity21284 units
Recall ReasonReports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
Device Classification20230705
Device Code InfoUDI/DI 14026704341501, Batch Numbers: 18GG16, 18HG10, 18HG25, 18IG03, 19BG12, 19BG16, 19CT42, 19CT64, 19DT36, 19ET09, 19ET31, 19ET53, 19GT02, 19IT38, 19JT21, 19JT55, 19KT20, 19KT37, 19LT31, 20AT40, 20DT01, 20DT20, 20ET30, 20GT38, KME20J3096, KME20K2145, KME20L1345, KME20M1802, KME21B0621, KME21B2379, KME21C0168, KME22A1495, KME22A2394, KME22A2396, KME22B2938, KME22C2668, KME22C2669, KME22C2687, KME22D3223, KME22E1149, KME22E2287, KME22G1233, KME22G1879, KME23B0133, KME23B0560, KME23B0717, KME23B2197
Center Classification Date20230629
Recall Initiation Date20230525
Recalling FirmTELEFLEX LLC
Initial Notification Letter
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