Nico Corp. recalls
Every recall we track for Nico Corp. — 3 in all, from 2018–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Nico Corp. 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 | 0 | 0 | 0 |
| 2021 | 0 | 2 | 0 | 0 | 2 |
| 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 Nico Corp. 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 Nico Corp. recalls
2 shown- Use cautionMedical device
Nico Corp. recalls Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection
Nico Corp. recalls Myriad-LX Light Sources with serial numbers 350-00194D to 350-00475D due to potential tissue damage from sleeve occlusion during surgery. Updated instructions prevent light output reduction and sleeve blockage.
Nico Corp.Apr 30, 2021 - Lower riskMedical device
Nico Corp. recalls NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024
Nico Corp. recalls NICO Shepherd's Hook (Part NN-8024) due to mislabeled pouch lacking critical product details like part numbers and expiration dates. Affected units sold with Lot 37LG1834 expiring Jan 2020.
Nico Corp.Jun 19, 2018
Nico Corp. recall questions
How many recalls has Nico Corp. had?
3 recalls from Nico Corp. are on record with U.S. safety agencies, from 2018–2021.
What is the most recent Nico Corp. recall?
Nico Corp. recalls Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection, dated Apr 30, 2021. Every Nico Corp. recall is listed on this page, newest first.
What should I do if I have a recalled Nico Corp. 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 Nico Corp. 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.