AESCULAP ER223RRecalls & reported problems
Aesculap AG · RECAMIER Uterine Curette, 11 3/4", (300 mm), rigid, sharp, Fig. 3, width: 12 mm, non-sterile, reusable · Class 1
Data updated Oct 16, 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 04038653041800), received between Feb 18, 2021 and Mar 25, 2021 — 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 16, 2026.
Most reported problems
Device problems
- Fracture2
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 25, 2021Fracture; Fracture
ADDITIONAL INFORMATION: THE PATIENT UNDERWENT A DILATION AND CURETTAGE FOR A MOLAR PREGNANCY. THE CURETTE FRACTURED, BROKE, CRACKED AND/OR SPLINTERED INSIDE OF THE PATIENT. DUE TO THIS MALFUNCTION, AN ABDOMINAL LAPAROSCOPY AND HYSTEROSCOPY WAS PERFORMED. FURTHER DETAILS WERE NOT PROVIDED.
Patient problems: Foreign Body In Patient
MAUDE report 11568164 ↗InjuryFeb 18, 2021Fracture; Fracture
THE PATIENT UNDERWENT A DILATION AND CURETTAGE FOR A MOLAR PREGNANCY. THE CURETTE FRACTURED, BROKE, CRACKED AND/OR SPLINTERED INSIDE OF THE PATIENT. DUE TO THIS MALFUNCTION, AN ABDOMINAL LAPAROSCOPY AND HYSTEROSCOPY WAS PERFORMED. FURTHER DETAILS WERE NOT PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11344714 ↗
Other CURETTE, UTERINE devices
- Sklar Instruments 96-4113Sklar Corporation · CURETTE, UTERINE1 recall0 reports
- AESCULAP ER402RAesculap AG · CURETTE, UTERINE2 reports
- Busse Hospital Disposables 284Robert Busse & CO., Inc. · Curette, Uterine1 report
- V. Mueller GL1625Steris Corporation · CURETTE, UTERINE1 report
- V. Mueller GL1600-003Steris Corporation · CURETTE, UTERINE1 report
- CARDINAL HEALTH SMA11LSJH3Cardinal Health 200, LLC · CURETTE, UTERINE1 report
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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