Extentrac Elite product brochure DCN: 13-001 — Class II medical device recall Z-1717-2015
Terminated recall by Advanced Back Technologies, Inc., reported 2015-06-17, distributed in CA, FL, NJ, TX, WA. Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patie
| Recall number | Z-1717-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advanced Back Technologies, Inc., Hauppauge, NY, United States |
| Recall initiated | 2015-05-13 |
| Classified | 2015-06-05 |
| Reported by FDA | 2015-06-17 |
| Terminated | 2018-05-23 |
| Distributed | CA, FL, NJ, TX, WA |
| Countries outside the US | AU, CA, CN, EG, GR, KR, KW, LB, RU, SA, TR |
| Quantity | 36 units |
| 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 and 11 more |
Product
Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1717-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.