FDAOctober 13, 2025device
TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.
What to do
FDA enforcement status: Ongoing
Brands named
tmj solutionstmj
UPCs
07613327626551076133276265680761332762657507613327626605
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- USDA FSISFSIS Issues Public Health Alert for Ravioli Pasta With Beef Sauce Due to Misbranding and Undeclared Allergens2026-05-04
- FDABW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDADaig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
- FDABARD Dynamic Tip Steerable, Product Number 6DYNTP001;2026-04-10
- FDADaig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
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