Innovasis, Inc recalls
Every recall we track for Innovasis, Inc — 4 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Innovasis, 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 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 1 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Innovasis, 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 Innovasis, Inc recalls
4 shown- Lower riskMedical device
Innovasis, Inc recalls Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System
Innovasis recalls LS-749 pedicle screw part for potential surgical delays. The anti-torque instrument may not engage properly during tightening, requiring alternative procedures.
InnovasisMay 22, 2026 - UnratedMedical device
Innovasis, Inc recalls TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion
Innovasis recalls specific spinal fusion implants due to interfacing issues between the implant trial and inserter, which could lead to improper device function during surgery.
InnovasisAug 14, 2024 - Lower riskMedical device
Innovasis, Inc recalls Oryx Cervical Screw Caddy, Model Number BTA-172, as part of the Oryx Cervical Plate System - Product Usage: The
Innovasis recalls Oryx Cervical Screw Caddy Model BTA-172 due to incorrect labeling of fixed and variable rescue screws, which could cause improper installation and interference with cover screws.
InnovasisApr 7, 2020 - Lower riskMedical device
Innovasis, Inc recalls Excella II Polyaxial Pedicle Screw used as a pedicle screw system in skeletally mature patients, is intended to provide
Innovasis recalls 9 lots of 8.5mm Polyaxial Pedicle Screws used in spinal fusion that may break during surgery, causing potential complications.
InnovasisJan 8, 2018
Innovasis, Inc recall questions
How many recalls has Innovasis, Inc had?
4 recalls from Innovasis, Inc are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Innovasis, Inc recall?
Innovasis, Inc recalls Anti-Torque, Vector, Part: LS-749 part of Vector Pedicle Screw System, dated May 22, 2026. Every Innovasis, Inc recall is listed on this page, newest first.
What should I do if I have a recalled Innovasis, 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 Innovasis, 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.