RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls
Every recall we track for RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) — 45 in all, from 2020–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) peaked in 2021 (41); 45 since 2017.
All FDA recall records for RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 4 | 0 | 4 |
| 2021 | 0 | 41 | 0 | 0 | 41 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls
4 shown- Use cautionMedical device
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 48mm Material Number: 66-348 - Product Usage: intended for
Pioneer Surgical Technology recalls CervAlign Anterior Cervical Plate System (3 Level, 48mm) due to locking mechanism disassociating during surgery or after. Affected units have specific batch numbers.
Pioneer Surgical TechnologyJan 15, 2021 - Lower riskMedical device
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls Streamline OCT Navigated Instruments, Catalog numbers 26-DRILL-MDN 26-FTAP-30-MDN 26-FTAP-35-MDN 26-FTAP-40-MDN
Pioneer Surgical Technology recalls Streamline OCT Navigated Instruments with catalog numbers 26-DRILL-MDN through 26-S-FINDER-MDN due to missing drill guide. This could lead to improper surgical procedures.
Pioneer Surgical TechnologySep 24, 2020 - Lower riskMedical device
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls Streamline TL Navigation System, Catalog Nos. 02-C-TAP-55-MDN 02-C-TAP-60-L-MDN 02-C-TAP-65-L-MDN 02-C-TAP-65-MDN
Pioneer Surgical recalls Streamline TL Navigation System devices with specific catalog numbers due to binding issues that may affect spinal surgery procedures.
Pioneer SurgicalSep 24, 2020 - Lower riskMedical device
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls Streamline MIS Navigation System Taps, Catalog numbers 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN
Pioneer Surgical Technology recalls Streamline MIS Navigation System Taps (catalog numbers 04-CANNDRILL-MDN, 04-CANNTAP-40-MDN, etc.) due to incompatibility with Streamline MIS tap sleeves. Affected units may cause improper function during surgery.
Pioneer Surgical TechnologySep 11, 2020
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recall questions
How many recalls has RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) had?
45 recalls from RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) are on record with U.S. safety agencies, from 2020–2021.
What is the most recent RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recall?
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls CervAlign Anterior Cervical Plate System-Cervalign, 3 Level, 48mm Material Number: 66-348 - Product Usage: intended for, dated Jan 15, 2021. Every RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recall is listed on this page, newest first.
What should I do if I have a recalled RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.