Device Recall TS Series Depth Gauge for Integra Ti6 Internal Fixation System 2.0/2.5mm Screws 의 리콜

Recall

74114

Class 2

Z-1965-2016

2016-05-10

Terminated

United States

2016-12-16

USFDA

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=146323

As a result of an internal investigation of a non-conformance it has been determined: 1) depth gauges from lot up15h2 exceed the overall length specification requirements. 2) depth gauges from prior lot numbers manufactured before integra acquired the product line reflect an incorrect number for the first mm depth marking on the gauge. the number should be 4, it is 6. 3) the space / holder.

The firm, Integra Lifesciences, sent an "Urgent: Voluntary Medical Device Recall" letter dated 5/10/16 to affected consignees/customers via traceable courier service on 5/10/16. The letter describes the product, problem and actions to be taken. The customers were instructed to stop using and distributing product immediately; complete and return the Recall Acknowledgement and Return Form via fax to 1-609-275-9445 or email to FCA2@integralife.com, even if you do not have any of the product. Should you have any questions, please contact Customer Service at 1-866-854-8300.