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Full Vision Inc

Complete recall history across all FDA and CPSC categories — 14 total recalls

Full Vision Inc appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (14)

FDA medical device enforcement actions by Full Vision Inc

Date Product Reason Class
May 12, 2023 TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928 Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
May 12, 2023 TRACKMASTER, TREADMILL TMX428 220V, MODEL NUMBER 317-07927 Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
May 12, 2023 TRACKMASTER, TREADMILL GE T2100-ST1 110VV, MODEL NUMBER 317-07926GE Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
May 12, 2023 TRACKMASTER, TREADMILL GE T2100-ST2 220V, MODEL NUMBER 317-07927GE Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
May 12, 2023 TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926 Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
May 12, 2023 TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929 Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
May 12, 2023 TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA Treadmill malfunction: drive PCB can misread the signals and stop or reverse... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER, TREADMILL TMX428 110V, Model #317-07926 This has been identified a rare occurrence, under a specific scenario, where ... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 110V, Model #317-07928 This has been identified a rare occurrence, under a specific scenario, where ... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE This has been identified a rare occurrence, under a specific scenario, where ... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST2 220V, Model #317-07927GE... This has been identified a rare occurrence, under a specific scenario, where ... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE This has been identified a rare occurrence, under a specific scenario, where ... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER,TREADMILL TMX428 220V, Model #317-07927 This has been identified a rare occurrence, under a specific scenario, where ... Class II
Aug 31, 2022 FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929 This has been identified a rare occurrence, under a specific scenario, where ... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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