Mani, Inc. - Kiyohara Facility recalls
Every recall we track for Mani, Inc. - Kiyohara Facility — 3 in all, from 2020–2023 — 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 Mani, Inc. - Kiyohara Facility 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 | 2 | 0 | 0 | 2 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 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 Mani, Inc. - Kiyohara Facility 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 Mani, Inc. - Kiyohara Facility recalls
2 shown- Lower riskMedical device
Mani, Inc. - Kiyohara Facility recalls Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3
Mani recalls two trocar kit models (MTK23S and MTK25S) due to potential packaging defects that could compromise sterile barriers. Affected kits were sold with specific lot numbers and expiration dates.
ManiFeb 20, 2023 - Use cautionMedical device
Mani, Inc. - Kiyohara Facility recalls MANI Infusion Cannula 23G S - Product Usage: for use in injecting perfusate or aspirating out intraocular materials
Mani recalls 23G S infusion cannulas for eye surgery due to potential fluid leakage and disconnection risks. Affected units have specific lot codes and expiration dates.
ManiOct 27, 2020
Mani, Inc. - Kiyohara Facility recall questions
How many recalls has Mani, Inc. - Kiyohara Facility had?
3 recalls from Mani, Inc. - Kiyohara Facility are on record with U.S. safety agencies, from 2020–2023.
What is the most recent Mani, Inc. - Kiyohara Facility recall?
Mani, Inc. - Kiyohara Facility recalls Mani Trocar Kit, Model MTK23S and Model MTK25S There are 3 kits contained in one box, and sterile 1 kit consists of 3, dated Feb 20, 2023. Every Mani, Inc. - Kiyohara Facility recall is listed on this page, newest first.
What should I do if I have a recalled Mani, Inc. - Kiyohara Facility 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 Mani, Inc. - Kiyohara Facility 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.