Centinel Spine, Inc. recalls
Every recall we track for Centinel Spine, Inc. — 6 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
6 recalls since 2017.
All FDA recall records for Centinel Spine, 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 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 1 | 1 | 2 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 2 | 0 | 2 |
What to do if you have a recalled Centinel Spine, 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 Centinel Spine, Inc. recalls
4 shown- Lower riskMedical device
Centinel Spine, Inc. recalls Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.
Centinel Spine recalls Prodisc C SK U.S. Implant Extra Large 5mm (Model PDSXL5) due to labeling error where 5mm and 6mm products were swapped. No action needed as it's a labeling issue, not a safety hazard.
Centinel SpineMar 20, 2026 - Lower riskMedical device
Centinel Spine, Inc. recalls Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description:
Centinel Spine recalls Prodisc C SK model PDSL6 due to mislabeling as 6mm but containing 5mm disc. Affected users should verify product details to avoid incorrect usage.
ProdiscDec 31, 2025 - UnratedMedical device
Centinel Spine, Inc. recalls prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5
Centinel Spine recalls Prodisc C SK cervical disc replacements with possible blue discoloration indicating foreign contamination. Affected units have model PDSM5 and lot 2024-0482. No remedy specified in official notice.
Centinel SpineJul 18, 2024 - Lower riskMedical device
Centinel Spine, Inc. recalls Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction
Centinel Spine recalls Prodisc C intervertebral disc implants missing the UP etching on the superior plate, which can lead to improper placement during surgery. Affected units sold from 2020-06-01.
Centinel SpineMar 5, 2021
Centinel Spine, Inc. recall questions
How many recalls has Centinel Spine, Inc. had?
6 recalls from Centinel Spine, Inc. are on record with U.S. safety agencies, from 2021–2026.
What is the most recent Centinel Spine, Inc. recall?
Centinel Spine, Inc. recalls Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement., dated Mar 20, 2026. Every Centinel Spine, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Centinel Spine, 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 Centinel Spine, 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.