TMJ Bilateral Implants
TMJ Solutions is recalling custom temporomandibular joint implants due to incorrect components causing a poor fit and potential open bite.
Contact your surgeon or healthcare provider immediately if you have experienced symptoms such as an open bite or discomfort following your TMJ implant procedure.
Why it was recalled
TMJ Solutions is recalling custom temporomandibular joint implants due to the inclusion of incorrect patient-specific components. This error may result in a poor fit of the device, which can lead to a right-sided open bite for the patient.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
TMJ Bilateral Implants, REF: CHG020
- UDI-DI
- 07613327626575, 2508181038
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Device Defect recalls
Editorial summary by Recall Canary · summary updated 2026-06-23 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification