Mizuho OSI recalls
Every recall we track for Mizuho OSI — 3 in all, from 2019–2021 — 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 Mizuho OSI 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 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 1 | 1 | 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 Mizuho OSI 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 Mizuho OSI recalls
3 shown- Lower riskMedical device
Mizuho OSI recalls HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
Mizuho OSI recalls HANA/PROFx Classic Femoral Hook Right Ref 6850-144 due to incorrect model numbering. Affected units have a specific batch code and require verification.
Mizuho OSIJul 29, 2021 - Use cautionMedical device
Mizuho OSI recalls Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage:
Mizuho OSI recalls specific surgical table hand control units that may cause the tabletop to slide in the opposite direction from user selection, potentially delaying procedures. Affected units have unique serial numbers listed in the recall notice.
MizuhoFeb 8, 2021 - Use cautionMedical device
Mizuho OSI recalls Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI -
Mizuho OSI recalls Levo Arm Label models 7887-050 and 7887-050R due to potential fluid ingress causing electrical failure and locking mechanism issues during spinal surgery. Affected units have serial numbers listed in the recall notice.
Mizuho OSIOct 14, 2019
Mizuho OSI recall questions
How many recalls has Mizuho OSI had?
3 recalls from Mizuho OSI are on record with U.S. safety agencies, from 2019–2021.
What is the most recent Mizuho OSI recall?
Mizuho OSI recalls HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144, dated Jul 29, 2021. Every Mizuho OSI recall is listed on this page, newest first.
What should I do if I have a recalled Mizuho OSI 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 Mizuho OSI 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.