FDA Medical Device Recalls (openFDA)
Advanced Back Technologies, Inc.: Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
- Recall number
- Z-1717-2015
- Recalling firm
- Advanced Back Technologies, Inc.
- Product
- Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
- Status
- Terminated
- Initiated
- 2015-05-13
- Posted
- 2015-06-05
- Terminated
- 2018-05-23
- Reason
- 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
- Root cause
- Error in labeling
- Action
- Advanced Back Technologies, Inc. sent an Urgent Medical Device Brocure & User Manual Recall letter dated May 13, 2015, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed the discard the DCN's identified as DCN 13-001, DCN 09-001, DCN 14-001 and replace with the newly issued DCN 15-001, DCN 15-002. The new DCN's would be provided to customers in pdf format via email for issuance. Customers were asked to contact their customers who purchased the affected product and inform them that they should not treat patients with a maximum weight exceeding 300 lbs until the firm is able to make an amendment to their 510(k). Customers with questions should call 631-231-0076.
- Quantity
- 36 units
- Distribution
- Worldwide Distribution - US including CA, FL, NJ, TX, WA, Internationally: Korea, Russia, Kuwait, Canada, Greece, Lebanon, Turkey, Egypt, Saudi Arabia, China, Armenia, Azerbaijan, Australia.
- Lot, serial or model codes
- 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
- 510(k) numbers
- ["K031996"]
- PMA numbers
- not on file
- Product code
- ITH
- Firm FEI
- 3004755153
- Firm city
- Hauppauge
- Firm state
- NY
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
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Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28