RTI Surgical Streamline Occipito-Cervico-Thoracic — Class II medical device recall Z-1393-2016
Terminated recall by RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.), reported 2016-04-20, distributed in AL, CO, CT, FL, ID, IL, IN, MI…. Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing du
| Recall number | Z-1393-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.), Marquette, MI, United States |
| Recall initiated | 2016-03-18 |
| Classified | 2016-04-14 |
| Reported by FDA | 2016-04-20 |
| Terminated | 2016-09-12 |
| Distributed | AL, CO, CT, FL, ID, IL, IN, MI, MO, MS, NC, NY, TX |
| Reason classes | potency |
| Lot numbers | 177091, 177093, 183817, 207727, 223926, 227291, 229134, 230523, 232262, 233074, 234205 |
Product
RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver
Reason for recall
Multiple lots of the 26-FNLDRIVER, may have reduced mechanical strength, resulting in driver tip fracturing during use.
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-1393-2016. 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.