ClearanceBrief
Recall Z-0129-2007 ยท LNZ Changer, Tube, Endotracheal

Teleflex Medical

Sheridan T.T.X. Tracheal Tube Exchanger, Large Size for tracheal tube sizes 7.5 mm - 10.0 mm; a Rx, sterile, single use tracheal tube exchanger; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-24006

DateNov 2, 2006 (initiated Sep 27, 2006)
StatusTerminated
ReasonBiological indicator failed. Investigation eliminated all equipment and product related factors.
Root causeOther
ActionTeleflex Medical sent Urgent Medical Device Recall letters dated 9/27/06 via UPS overnight to the direct accounts, informing them that the product did not pass validated sterility test requirements, and requesting that they cease use of the affected units and return them to Teleflex Medical for replacement. If the accounts further distributed the product, they were requested to conduct a sub-recall of the affected units from their customers. The accounts were instructed to complete and return by fax the enclosed Acknowledgement & Stock Status Form, indicating the number of units being returned
Quantity80 units
DistributionNationwide and Argentina, Canada, Chile, Japan, Malaysia, the Netherlands and New Zealand
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K862347ENDOTRACHEAL TUBE, ACCESSORY
Sheridan Catheter Corp., Jul 11, 1986