TMJ Solutions Inc recalls TMJ Bilateral Implants, REF: CHG020
See all recalls from TMJ Solutions Inc →Recalled Product
TMJ Bilateral Implants, REF: CHG020
Hazard / Issue
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 07613327626575, Lot: 2508181038
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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