Pipet Curet MX140Recalls & reported problems
Coopersurgical, Inc. · Endometrial suction curette · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888937003536), received between Oct 10, 2018 and Oct 10, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Most reported problems
Device problems
- Break1
- Detachment of Device or Device Component1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 10, 2018Break; Detachment of Device or Device Component
TIP OF CURETTE BROKE OFF DURING PROCEDURE. WAS RETRIEVED, NO INJURY TO PATIENT. 3MM PIPET CURETTE BOX 50 MX140 (B)(4).
Patient problems: Foreign Body In Patient
MAUDE report 7952094 ↗
Other Curette, Suction, Endometrial (And Accessories) devices
- BERKELEY VC-10Gyrus ACMI, LLC · Curette, Suction, Endometrial (And Accessories)1 recall8 reports
- BERKELEY SAFE-TOUCH 003853-902Gyrus ACMI, LLC · Curette, Suction, Endometrial (And Accessories)8 reports
- Gyrus ACMI 23116Gyrus ACMI, LLC · Curette, Suction, Endometrial (And Accessories)3 reports
- SAFETOUCH 003984-901Gyrus ACMI, LLC · Curette, Suction, Endometrial (And Accessories)2 reports
- Gyrus ACMI 54298Gyrus ACMI, LLC · CURETTE, SUCTION, ENDOMETRIAL (AND ACCESSORIES)2 reports
- Berkeley Vacurette 21593AGyrus ACMI, LLC · Curette, Suction, Endometrial (And Accessories)1 report
- Uterine Explora Curette - Model I MX120Coopersurgical, Inc. · Curette, Suction, Endometrial (And Accessories)1 report
- Gyrus ACMI 003997-901Gyrus ACMI, LLC · Curette, Suction, Endometrial (And Accessories)1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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