Skip to content
Recall Observatory FDA recall evidence

Device product

OptiLITE(TM) Products for Laser Surgery, Catalog Numbers: HTM1020F, HTM1040F, HTM1060F, HTM1010F; Manufactured by CONVERGENT LASTER TECHNOLOGIES The Odyssey 30B is approved for numerous medical procedures. Generally, the primary use of the laser (which includes the fibers) is related to urology, but ultimately it is up to the surgeon except in cases where it is contraindicated. The fibers are usually used in cases involving stones anywhere from the bladder up to the kidneys. Occasionally the laser system is used in soft tissue cases (non-cancerous tumors) in and around the urinary system.

Z-2866-2017

June 23, 2017

Class II

Product summary

Firm
Xintec Corp
Event
Event 77653
Status
Terminated
Classification
Class II
Quantity
4343 units
Official record key
device-enforcement:Z-2866-2017

Official wording

Reason: It has been determined that the reprocessing instructions may not provide sufficiently detailed information for the cleaning, disinfection and sterilization of the products listed below. The preliminary investigation indicates that validation data related to the reprocessing of these devices may not meet newly enacted standards.

Code information: all codes.

Distribution pattern: Worldwide distribution- US (Nationwide) and countries of: Canada and Sri Lanka.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    It has been determined that the reprocessing instructions may not provide sufficiently detailed information for the cleaning, disinfection and sterilization of the products listed below. The preliminary investigation indicates that validation data related to the reprocessing of these devices may not meet newly enacted standards.