PIPELINE 288205046Recalls & reported problems
Depuy Spine, LLC · PIPELINE ACCESS SYSTEM CURETTE, RIGHT ANGLE 6.5mm · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034220468), received between Oct 21, 2022 and Nov 20, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 20, 2025Break; Break
BREAKAGE. IT WAS REPORTED THAT DURING THE SURGERY, THE HANDLE AND JOINT OF THE DEVICE WERE BROKEN INTO TWO PIECES DIRECTLY (AS THE ATTACHED PHOTO SHOWS). ANOTHER DEVICE WAS USED TO COMPLETE THE SURGERY. THERE WERE NO ADVERSE CONSEQUENCES TO THE PATIENT. NO ADDITIONAL INFORMATION COULD BE PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23605900 ↗MalfunctionOct 21, 2022Break; Break
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN JAPAN AS FOLLOWS: IT WAS REPORTED THAT THE HANDLE OF THE ANGLE CURETTE IN QUESTION WAS BROKEN WHEN IT WAS DELIVERED TO THE AGENT ON SEPTEMBER 30, 2022. THE ANGLE CURETTE WAS PREPARED FOR SURGERY ON (B)(6) 2022. THE BREAKAGE WAS FOUND BEFORE THE ANGLE CURETTE WAS DELIVERED TO THE HOSPITAL. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE PIPELINE ACCESS SYSTEM CURETTE, RIGHT ANGLE 6.5MM . THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15651066 ↗
Other CURETTE devices
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- Centurion I68040Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68380Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67050Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68340Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I67970Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68480Centurion Medical Products Corporation · CURETTE1 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 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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