BTE TECHNOLOGIES
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (3)
Devices registered here (1)
- Exerciser, MeasuringProduct code ISD (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5360
Recalls & enforcement
- Class IITerminated2015-04-09On the Primus that includes the optional Chop / Lift Bar, there is a remote possibility that the Chop / Lift Bar could get accidently detached from the snap hook in specific use scenarios when the bar is rotated and twisted around the snap hook. The snap hook could open, resulti…
FDA inspections (3)
- NAI2026-06-29No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
- VAI2020-01-31Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- VAI2016-02-26Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “BTE TECHNOLOGIES (FEI 1119903) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1119903-bte-technologies/
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