MR8 Tools MR8-10MH30SHRecalls & reported problems
Medtronic Powered Surgical Solutions · TOOL MR8-10MH30SH 10CM MATCH 3MM SHORT · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000447298), received between Nov 10, 2023 and Nov 10, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Dull, Blunt” (1 report).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Dull, Blunt1
- No Apparent Adverse Event1
- Overheating of Device1
- Smoking1
Patient problems
- Burn(s)1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 10, 2023Overheating of Device; Smoking; Dull, Blunt; No Apparent Adverse Event; Overheating of Device; Smoking; Dull, Blunt; No Apparent Adverse Event
ON FOLLOW UP IT WAS REPORTED THAT THERE WAS NO PATIENT OR STAFF IMPACT. FURTHER IT WAS REPORTED THAT THERE WAS A DELAY IN SURGICAL PROCEDURE OF 15 MINUTES BECAUSE THE SURGEON WAS ADAMANT TO SWITCH MICROSCOPES SO A VIDEO COULD BE MADE ON A CLEAR SCREEN TO SEND IN.
Patient problems: Burn(s); No Clinical Signs, Symptoms or Conditions
MAUDE report 18111185 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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