STREAMLINE CT CERVICO-THORACIC SYSTEM — Class II medical device recall Z-2573-2014
Terminated recall by PIONEER SURGICAL TECHNOLOGY, INC., reported 2014-09-10, distributed in CA, FL, IL, MI, NC, NH, NY. Some set screw thread profiles were found not to be within specifications.
| Recall number | Z-2573-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | PIONEER SURGICAL TECHNOLOGY, INC., Marquette, MI, United States |
| Recall initiated | 2012-09-10 |
| Classified | 2014-09-03 |
| Reported by FDA | 2014-09-10 |
| Terminated | 2014-09-30 |
| Distributed | CA, FL, IL, MI, NC, NH, NY |
| Quantity | 11 sets |
| Lot numbers | 104875, 104876, 104877, 104878, 104879, 104880, 104881, 117030, 117031, 121947, 124260 |
| Model numbers | 26-SETSCREW |
Product
STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE, SINGLE USE, RX ONLY
Reason for recall
Some set screw thread profiles were found not to be within specifications.
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-2573-2014. 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.