AESCULAP MG211RRecalls & reported problems
Aesculap, Inc. · , non-sterile, reusable · 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 04046964687334), received between Apr 4, 2023 and Apr 4, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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.
Most reported problems
Device problems
- Fracture1
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.
InjuryApr 4, 2023Fracture; Fracture
IT WAS REPORTED TO AESCULAP INC. THAT UTERINE SCISSORS ANGLED 265MM (PRODUCT # MG211R) WERE USED DURING A RIGHT PERIACETABULAR OSTEOTOMY (PAO), ALSO CALLED A BERNESE OR GANZ PROCEDURE, ON (B)(6), 2023. ACCORDING TO THE COMPLAINANT, DURING THE PROCEDURE, THE SCISSORS BROKE IN HALF. ADDITIONAL INFORMATION REVEALED THAT A PORTION OF THE DEVICE BROKE OFF WITHIN THE PATIENT, BUT WAS ABLE TO BE SUCCESSFULLY RETRIEVED. ALTHOUGH THE PATIENT REPORTEDLY SPENT ADDITIONAL TIME UNDER ANESTHESIA DUE TO THE RETRIEVAL, THE LENGTH OF THE DELAY WAS NOT SPECIFIED. THE COMPLAINT DEVICE HAS BEEN RETURNED TO THE MANUFACTURER FOR EVALUATION. THE ADVERSE EVENT/MALFUNCTION IS FILED UNDER AIC REFERENCE: (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16675607 ↗
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- Centurion I68790Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66150Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66350Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 67645Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 reports
- Centurion 66710Centurion Medical Products Corporation · SCISSORS, GENERAL, SURGICAL1 recall0 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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