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Howmedica Osteonics Corp. recalls Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and minim
Recalled December 19, 2018 · FDA recall Z-0605-2019 · Howmedica Osteonics
Hazard
The surgical technique is being updated to caution against misuse due to reports of cage fractures occurring intra-operatively and post-operatively. · FDA Class II
Units
28,461
Sold at
US Nationwide
Description
The surgical technique is being updated to caution against misuse due to reports of cage fractures occurring intra-operatively and post-operatively.
Product
Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and minimally invasive PLIF or TLIF surgical procedure.
Manufacturer(s)
Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →