Reported Jun 17, 2015 · Terminated
Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
Advanced Back Technologies, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Advanced Back Technologies, Inc. · 89 Cabot Ct Ste F · Hauppauge, NY · 11788-3719
Is this the product you have?
- Extentrac Elite product brochure DCN
13-00109-001 (Powered decompression tablefor traction)
- Lot codes and dates
- Serial Numbers
00500601101701907011010707100307071004080310050808100608091007090610090909101009101011091010121002101410031015100910171012101911051020110610211107102211091023120110261208102813021028120910291209103012121032130110331310103413071037130310351401103814041036 and 14061038
- Serial Numbers
- Amount recalled
- 36 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was 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
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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