TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI: (01)07613327626575/ 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
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- TMJ Solutions Inc
- Reason for Recall:
- Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
Product Codes/Lot Numbers:
UDI: (01)07613327626575/ 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
Distribution:
Distributed in: US, IL, OR, MS, TX, OK, UT, MA, MD, NY, PA, VA, FL, CA, MN, GA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0488-2026
Related Recalls
Patient-fitted temporomandibular (TMJ) prothesis contained incorrect components, SterileEO
This device was mislabeled and is not the correct component for this patient.