AESCULAP GD675Recalls & reported problems
Aesculap AG · microspeed uni XS Hi · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04038653347605), received between Dec 5, 2019 and Mar 23, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (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.
Most reported problems
Device problems
- Display or Visual Feedback Problem1
- Excessive Heating1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 23, 2021Display or Visual Feedback Problem; Mechanical Problem; Display or Visual Feedback Problem; Mechanical Problem
NEW INFORMATION: AT 9:00 AM ON (B)(6) 2021, CHECKED MICROSPEED MOTOR SYSTEM OF BBRAUN BEFORE ORTHOPEDIC SURGERY AND FOUND THAT THE POWER ON SCREEN OF THE EQUIPMENT WAS NORMAL. CONNECTED THE HIGH-SPEED MOTOR LEAD LINE GD675. WHEN THE DEVICE PEDAL WAS DOWN, ERROR 9 APPEARED ON THE HOST SCREEN, AND GD675 HIGH-SPEED MOTOR DID NOT ROTATE. PLUGGED IN THE INTERFACE, RESTARTED THE DEVICE SYSTEM SEVERAL TIMES, THE FAULT HAD NOT BEEN ELIMINATED. AS THE PATIENT HAD ENTERED THE OPERATING ROOM TO START ANESTHESIA, THE EQUIPMENT WAS STOPPED AFTER ASKING FOR INSTRUCTIONS. REPLACED SPARE EQUIPMENT AND PROVIDED IT TO DOCTORS FOR OPERATION. NO HARM HAD BEEN DONE TO THE PATIENT. NO SAMPLE OR PICTURE PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11553121 ↗MalfunctionDec 5, 2019Excessive Heating; Excessive Heating
IT WAS REPORTED THAT THERE WAS AN ISSUE WITH THE PRODUCT MICROSPEED UNI XS HIGHSPEED MOTOR. AS PER RECEIVED INFORMATION THE DRILL IS OVERHEATING AND BURNED THE USER'S HAND; REPORTEDLY, THE BURN WAS SUPERFICIAL. ADDITIONAL INFORMATION WAS REQUESTED BUT IS NOT YET AVAILABLE. THE MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).
Patient problems: No Patient Involvement
MAUDE report 9418926 ↗
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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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