ClearanceBrief
Recall Z-1836-2015 ยท NLM Laparoscope, General & Plastic Surgery, Reprocessed

Stryker Sustainability Solutions

Cannula and Seal; 5mm x 100mm and 12mm x 100mm Model #: CTS02 and CTS22. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.

DateJun 25, 2015 (initiated Jun 1, 2015)
StatusTerminated
ReasonStryker Sustainability Solutions is recalling Trocars because they have received reports indicating that some may fracture at the distal tip resulting in fragments at the surgical site.
Root causeUnder Investigation by firm
ActionOn 06/01/15 a customer notification letter was sent out by the firm. The notification letter instructs customers to stop using the affected lots of the recalled product, and should consider other trocar models reprocesses by Stryker as an alternative. The letter notes that attached is a Effectiveness Check Form and complete list of affected lots shipped to the facility. A Stryker Sustainability Solutions Sales Representative will be sent to check the inventory of the affected lots. Once the inventory is checked the affected lots will be removed. The firm will complete a Recall Effectivene
Quantity147,351
DistributionDistributed Nationwide including Puerto Rico.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K063788REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS
Ascent Healthcare Solutions, Oct 15, 2007