Class II — PIONEER SURGICAL TECHNOLOGY, INC.
| Recalling firm | Pioneer Surgical Technology, Inc. |
|---|---|
| Registered facility | Pioneer Surgical Technology, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Some set screw thread profiles were found not to be within specifications. |
| Product | STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE, SINGLE USE, RX ONLY |
| Quantity | 11 sets |
| Distribution | Distributed in the states of NC, NH, NY, CA, MI, IL, and FL. |
| Initiated | 2012-09-10 |
| Classified | 2014-09-03 |
| Terminated | 2014-09-30 |
| Recall number | Z-2573-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — PIONEER SURGICAL TECHNOLOGY, INC. (Z-2573-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69033/
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