Uterine Explora Curette - Model I MX120Recalls & reported problems
Coopersurgical, Inc. · 3mm OD Curette with Vacu-Lok Syringe · Class 2
Data updated Oct 18, 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 00888937003505), received between Jul 11, 2025 and Jul 11, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Use of Device Problem1
Patient problems
- Bacterial Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 11, 2025Use of Device Problem; Detachment of Device or Device Component; Use of Device Problem; Detachment of Device or Device Component
IT WAS REPORTED BY THE USER FACILITY VIA MEDWATCH: ON [REDACTED] 2024, THE PATIENT WAS IN THE OFFICE AND HAD A SIS PROCEDURE TO EVALUATE POST-MENOPAUSAL BLEEDING. THE PATIENT UNDERWENT A PELVIC SONOGRAM AND A UTERINE BIOPSY. NO COMPLICATIONS WERE NOTED. ON [REDACTED] 2025, THE PATIENT SENT A MESSAGE TO THE OFFICE THAT SHE HAD A YELLOW PLASTIC CLIP COME OUT OF HER VAGINA WHILE IN THE SHOWER FOLLOWING INTERCOURSE. SHE HAD REPORTED THAT HER HUSBAND MENTIONED FEELING A HARD OBJECT INSIDE OF HER VAGINA WITH INTERCOURSE PREVIOUSLY. THE PATIENT WAS SEEN IN THE OFFICE FOR HER ANNUAL EVALUATION TO EVALUATE FURTHER, IT DOES NOT APPEAR THERE WAS SIGNIFICANT INJURY. THE PATIENT WAS DIAGNOSED WITH BACTERIAL VAGINITIS AT THE FOLLOW UP APPOINTMENT AND TREATED WITH DOXYCYCLINE. MX120 UTERINE EXPLORA (B)(4).
Patient problems: Bacterial Infection
MAUDE report 22479256 ↗
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
- Pipet Curet MX140Coopersurgical, Inc. · Curette, Suction, Endometrial (And Accessories)1 report
- Berkeley Vacurette 21593AGyrus ACMI, LLC · 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.
How reports and recalls are matched · Editorial policy · Report an error on this page