MBI Implant NM-V2910Recalls & reported problems
Noris Medical Ltd · MBI, D2.9, L10, Mini Ball Ti. Implant · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07290108814514), received between Mar 8, 2026 and Mar 9, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- Failure of Implant2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 9, 2026Fracture
THE IMPLANT WAS REMOVED DURING IMPLANT PLACEMENT DAY ON (B)(6) 2025 . OBSERVED DURING THE EVENT: IMPLANT BOLL TOP BROKE. THE MALFUNCTION DID NOT CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY. NO PATIENT OPERATIVE OR POST-OPERATIVE COMPLICATIONS REPORTED. WAS RETURNED WRONG DEVICE FOR ANALYSIS, IT DOES NOT MATCH THE STICKER AND LOT.
Patient problems: Failure of Implant
MAUDE report 24542559 ↗InjuryMar 8, 2026Fracture
THE IMPLANT WAS REMOVED DURING IMPLANT PLACEMENT DAY ON (B)(6) 2025. OBSERVED DURING THE EVENT: IMPLANT BOLL TOP BROKE. THE MALFUNCTION DID NOT CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY. NO PATIENT OPERATIVE OR POST-OPERATIVE COMPLICATIONS REPORTED. WAS RETURNED WRONG DEVICE FOR ANALYSIS, IT DOES NOT MATCH THE STICKER AND LOT.
Patient problems: Failure of Implant
MAUDE report 24541737 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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