FDA Device recall Z-1718-2015
Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction)
- FDA Device
- Class II
- terminated
- Published 2015-06-17
On 2015-06-17 the FDA classified a Class II recall of Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction) by Advanced Back Technologies, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1718-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-13 |
| Published | 2015-06-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Advanced Back Technologies |
| Distribution | CA, FL, NJ, TX, WA |
Product
Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction)
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
Identifiers
| code_info | Serial Numbers: 005, 006, 011, 017, 019, 0701101, 07071003, 07071004, 08031005, 08081006, 08091007, 09061009, 09091010,…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1718-2015%22
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