Reported Nov 26, 2025 · Ongoing

TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only

TMJ Solutions Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: TMJ Solutions Inc · 6059 King Dr · Ventura, CA · 93003-7607

Is this the product you have?

  • TMJ Bilateral Implant REFCHG020 Sterile EO, Rx Only
Lot codes and dates
  • UDI07613327626551,07613327626568,07613327626575,07613327626605,07613327627749 07613327627848/ Lot #s:
    • 2410301062
    • 2306091054
    • 2312121078
    • 2401181023
    • 2401231058
    • 2403191046
    • 2404291064
    • 2405021079
    • 2407221023
    • 2407241032
    • 2408081047
    • 2408131037
    • 2408161043
    • 2409031033
    • 2409241016
    • 2410011097
    • 2410071065
    • 2410091014
    • 2410111030
    • 2410291062
    • 2411111012
    • 2411121044
    • 2411201015
    • 2412061031
    • 2412121062
    • 2412201009
    • 2501021011
Amount recalled
63 units

Where it was sold

Why it was recalled

Stop using this product now

Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:17 PM UTC

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