ClearanceBrief
Recall Z-1682-2019 ยท BTR Tube, Tracheal (W/Wo Connector)

Teleflex Medical

RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

DateApr 1, 2019
StatusTerminated
ReasonThe firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
Root causeProcess control
ActionThe firm initiated the recall by letter on 04/01/2019. The letter stated reason for the recall and requested the return of the recalled units. Distributors were directed to collect the recalled units from their customers, consolidate them, and complete and return the acknowledgement form. The recalled units will be returned.
Quantity1787 units
DistributionNationwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K935842RUSCH LASERTUBUS/RUSCH LASER RESISTANT CUFFED WITH MURPHY EYE
Rusch, Inc., May 23, 1995