Treadmill Recalled for Drive PCB Malfunction Causing Unexpected Belt Movement
Full Vision Inc is recalling approximately 565 TrackMaster TMX428 treadmills due to a drive circuit board malfunction that can cause the belt to unexpectedly stop, reverse, or accelerate, posing a risk of falls or injury.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II medical device recall for a risk-of-harm product where no injuries have been reported to date. The potential for user falls due to unexpected treadmill belt malfunction places this recall in the High severity category.
Plain-English summary
Full Vision Inc is recalling approximately 565 units of the TrackMaster TMX428 110V treadmill (Model Number 317-07926) distributed nationwide in the United States and in 28 other countries worldwide. The affected units have specific serial numbers ranging from FVDC-7585 through FVDC-8863, with some numbers in this range excluded.
The treadmill's drive circuit board (PCB) contains a defect that causes it to misread electrical signals. When this occurs, the treadmill belt may unexpectedly stop running, reverse direction, or suddenly accelerate forward. These abrupt, unintended changes in belt movement create a serious risk of falls and injury to users.
If you own an affected treadmill, discontinue use immediately. Check your unit's serial number against the manufacturer's list of recalled models. Contact Full Vision Inc for information about repair options, replacement, or return.
The recalled product
- Product
- TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926
- Manufacturer
- Full Vision Inc
- Affected units
- 565
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- UDI/DI 00860176000606
- Serial Numbers: FVDC-7585
- FVDC-7586
- FVDC-7587
- FVDC-7588
- FVDC-7589
- FVDC-7590
- FVDC-7591
- FVDC-7592
- FVDC-7593
- FVDC-7594
- FVDC-7595
- FVDC-7596
- FVDC-7597
- FVDC-7598
- FVDC-7599
- FVDC-7600
- FVDC-7601
- FVDC-7603
- FVDC-7604
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 7 recalled by Full Vision Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
Same manufacturer · Full Vision Inc
See all →- HighTrackMaster TMX428 Treadmill drive circuit board malfunction recall
FDA (Devices) · 2023-07-12
- HighTrackMaster Treadmill Recalled for Drive PCB Malfunction Risk
FDA (Devices) · 2023-07-12
- HighTreadmill recalled for drive PCB malfunction causing unexpected acceleration
FDA (Devices) · 2023-07-12
- HighTrackMaster GE Treadmill Recall Due to Drive Circuit Board Malfunction
FDA (Devices) · 2023-07-12
- HighTrackMaster Treadmill Drive PCB Malfunction Causes Unexpected Stop, Reverse, and Acceleration
FDA (Devices) · 2023-07-12
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