FDA Device recall Z-2573-2014
STREAMLINE CT CERVICO-THORACIC SYSTEM
- FDA Device
- Class II
- terminated
- Published 2014-09-10
On 2014-09-10 the FDA classified a Class II recall of STREAMLINE CT CERVICO-THORACIC SYSTEM by Pioneer Surgical Technology, citing some set screw thread profiles were found not to be within specifications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2573-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-10 |
| Published | 2014-09-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Pioneer Surgical Technology |
| Distribution | CA, FL, IL, MI, NC, NH, NY |
Product
STREAMLINE CT CERVICO-THORACIC SYSTEM; SET SCREW REF 26-SETSCREW NON-STERILE, SINGLE USE, RX ONLY
Reason
Some set screw thread profiles were found not to be within specifications.
Identifiers
| code_info | Lot numbers: 104875, 104876, 104877, 104878, 104879, 104880, 104881 , 117030,117031 , 121947, 124260. |
|---|
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-2573-2014%22
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