ClearanceBrief
Recall Z-2322-2021 ยท BTR Tube, Tracheal (W/Wo Connector)

Teleflex Medical Europe Ltd

RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055 c) 112082060 d) 112082065 e) 112082070 f) 112082075 g) 112082080 h) 112082085 i) 112082090 j) 112082095 k) 112082100

DateJul 16, 2021
StatusTerminated
ReasonThe firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
Root causeProcess control
ActionThe firm initiated the recall by letter on 07/16/2021. The letter explained the issue and requested the return of the product. Distributors were directed to notify their customers.
Quantity638220 units
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K961837RUSH ORAL/NASAL TRACHEAL TUBE CUFFED MAGILL/MURPHY
Rusch Intl., Aug 16, 1996