Full Vision Inc TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
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According to the U.S. Food and Drug Administration (FDA)
Product
TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928
Brand
Full Vision Inc
Lot Codes / Batch Numbers
UDI/DI 00860176000620, Serial Numbers: FVDC-7644, FVDC-7645, FVDC-7646, FVDC-7686, FVDC-7786, FVDC-7888, FVDC-7927, FVDC-8192, FVDC-8255, FVDC-8310, FVDC-8316, FVDC-8317, FVDC-8318, FVDC-8319, FVDC-8320, FVDC-8321, FVDC-8322, FVDC-8323, FVDC-8324, FVDC-8325, FVDC-8386, FVDC-8387, FVDC-8416, FVDC-8542, FVDC-8543, FVDC-8544, FVDC-8545, FVDC-8546, FVDC-8547, FVDC-8617, FVDC-8618, FVDC-8731, FVDC-8802, FVDC-8809, FVDC-8810, FVDC-8812, FVDC-8813, FVDC-8815, FVDC-8816
Products Sold
UDI/DI 00860176000620, Serial Numbers: FVDC-7644, FVDC-7645, FVDC-7646, FVDC-7686, FVDC-7786, FVDC-7888, FVDC-7927, FVDC-8192, FVDC-8255, FVDC-8310, FVDC-8316, FVDC-8317, FVDC-8318, FVDC-8319, FVDC-8320, FVDC-8321, FVDC-8322, FVDC-8323, FVDC-8324, FVDC-8325, FVDC-8386, FVDC-8387, FVDC-8416, FVDC-8542, FVDC-8543, FVDC-8544, FVDC-8545, FVDC-8546, FVDC-8547, FVDC-8617, FVDC-8618, FVDC-8731, FVDC-8802, FVDC-8809, FVDC-8810, FVDC-8812, FVDC-8813, FVDC-8815, FVDC-8816
Full Vision Inc is recalling TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 due to Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.
Recommended Action
Per FDA guidance
Trackmaster issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees beginning on 05/12/2023 by letter. The notice explained the problem and the risk during use, and requested the following: Immediate Actions to be taken by Customer/User: These steps are the recommendation of the Manufacturer to prevent injury and allow use of the device. Step 1: Instruct patient to straddle the belt and hold on to the handrails during initialization of the treadmill before starting the test Step 2: Send start/run command to the treadmill with patient still straddling the belt, wait 30 seconds to ensure there is no uncommanded motion Step 3: Instruct patient to carefully step on the belt while holding on to the handrails, begin walking and continue with the test Step 4: Patients unable to perform steps 1-3 must not use the treadmill Step 5: Print Appendix B and attach to the treadmill until corrections are made and ensure it is visible to the clinician and user
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026