Home / Recalls / Medical Devices
Spine Smith Partners LP recalls Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Recalled March 20, 2013 · FDA recall Z-0932-2013 · Spine Smith Partners
Hazard
Implants were incorrectly laser marked as 23mm instead of 28mm. · FDA Class II
Units
3 units
Sold at
Distributed in Texas.
Description
Implants were incorrectly laser marked as 23mm instead of 28mm.
Product
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Manufacturer(s)
Spine Smith Partners LP
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →