Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Extentrac Elite product brochure DCN: 13-001 Recalled by Advanced Back Technologies, Inc. Due to Item is marketed for use in patients weighing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Advanced Back Technologies, Inc. directly.
Affected Products
Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
Quantity: 36 units
Why Was This Recalled?
Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs
Where Was This Sold?
This product was distributed to 5 states: CA, FL, NJ, TX, WA
About Advanced Back Technologies, Inc.
Advanced Back Technologies, Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report