TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
- Company
- Tmj Solutions Inc
- Recall Initiated
- October 13, 2025
- Posted
- November 14, 2025
- Recall Number
- Z-0488-2026
- Quantity
- 27 units
- Firm Location
- Ventura, CA
Reason for Recall
Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.
Distribution
US: IL, OR, MS, TX, OK, UT, MA, MD, NY, PA, VA, FL, CA, MN, GA OUS: Canada, Spain, Brazil,
Lot / Code Info
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
Root Cause
Process control
Action Taken
On September 30, 2025 Stryker (TMJ Solutions) issued a "Urgent: Medical Device Recall" notification to affected consignees. On December 4, 2025, TMJ issued a expansion notification to additional consignees. TMJ Solutions asked consignees to take the following actions: 1. Inform individuals within your organization who need to be aware of this action. 2. Check your internal inventory to locate the affected product (Attachment B). Segregate the affected products, quarantine and discontinue use. 3. Please complete the Business Reply Form or use the QR Code on Attachment A. Response is required. a. If you have indicated that product remains in your inventory, a prepaid shipping label will be issued for the return of the product. Credit will be issued to your facility for products returned upon receipt. 4. Maintain awareness of this communication internally until all required actions have been completed within your facility .