POWERSPEED AS1 2305001Recalls & reported problems
Richard Wolf GmbH · MOTOR CONTROL UNIT 2305 for Orthopedics, Spine surgery and Bronchoscopy, for connection of motor handle M4. M5/0. M5/3. S1. M1 and High-Speed Motor X1, connection for two handpieces and a footswitch, 6.5" Touch Screen color display, compatible with core nova, U: 100-240VAC, 50/60Hz, Dim. (wxhxd): 300x159.5x404mm · Class 1
Data updated Oct 13, 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 04055207056660), received between May 27, 2025 and May 27, 2025 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Display or Visual Feedback Problem1
Patient problems
- 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.
InjuryMay 27, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem
THE CUSTOMER REPORTED THE FOLLOWING: DURING THE PATIENT'S ANESTHESIA, SHORTLY BEFORE THE SCHEDULED SURGERY, AN ERROR MESSAGE APPEARED WHEN ATTEMPTING TO CONNECT THE DRILL TO THE SHAVER SYSTEM. THIS RESULTED IN THE PATIENT'S AWAKENING AND THE CANCELLATION OF THE PROCEDURE. THERE WERE NO REPORTED INJURIES TO PATIENT/USERS OR THIRD PARTIES. NO INFORMATION IS AVAILABLE ABOUT THE TYPE OF PROCEDURE, OR THE MEASURES TAKEN DURING THE INCIDENT. HOWEVER, AS THE PROCEDURE WAS ABORTED, THE THREE SUBSEQUENT PROCEDURES WERE ALSO CANCELLED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22088908 ↗
Other MOTOR, SURGICAL INSTRUMENT, AC-POWERED devices
- NA 05.001.201Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED1,902 reports
- NA 530.710Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED1,800 reports
- NA 530.705Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED1,492 reports
- NA 530.715Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED390 reports
- NA 530.730Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED267 reports
- NA 05.001.240Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED262 reports
- KINCISE™ 1000-00-101Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED242 reports
- NA 530.791Synthes GmbH · MOTOR, SURGICAL INSTRUMENT, AC-POWERED84 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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