Clarus Medical, Llc recalls
Every recall we track for Clarus Medical, Llc — 1 in all, all from 2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
1 recall since 2017.
All FDA recall records for Clarus Medical, Llc 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 | 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 Clarus Medical, Llc 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 Clarus Medical, Llc recalls
1 shownClarus Medical, Llc recall questions
How many recalls has Clarus Medical, Llc had?
1 recall from Clarus Medical, Llc are on record with U.S. safety agencies, from 2021.
What is the most recent Clarus Medical, Llc recall?
Clarus Medical, Llc recalls Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002, dated Jul 27, 2021. Every Clarus Medical, Llc recall is listed on this page, newest first.
What should I do if I have a recalled Clarus Medical, Llc 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 Clarus Medical, Llc 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.