Advanced Back Technologies, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1717-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)

Product Classification:

Class II

Date Initiated: May 13, 2015

Date Posted: June 17, 2015

Recall Number: Z-1717-2015

Event ID: 71058

Reason for Recall:

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

Status: Terminated

Product Quantity: 36 units

Code Information:

Serial Numbers: 005, 006, 011, 017, 019, 0701101, 07071003, 07071004, 08031005, 08081006, 08091007, 09061009, 09091010, 09101011, 09101012, 10021014, 10031015, 10091017, 10121019, 11051020, 11061021, 11071022, 11091023, 12011026, 12081028, 13021028, 12091029, 12091030, 12121032, 13011033, 13101034, 13071037, 13031035, 14011038, 14041036 and 14061038

Distribution Pattern:

Worldwide Distribution - US including CA, FL, NJ, TX, WA, Internationally: Korea, Russia, Kuwait, Canada, Greece, Lebanon, Turkey, Egypt, Saudi Arabia, China, Armenia, Azerbaijan, Australia.

Voluntary or Mandated:

Voluntary: Firm initiated