MOSS 274220000Recalls & reported problems
Depuy Spine, LLC · MOSS INTRADISCAL INSTRUMENTS RING CURETTE SIZE 0 250mm · Class 1
All models of MOSS (16)
Data updated Oct 16, 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 10705034191720), received between Apr 23, 2020 and Apr 23, 2020 — 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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2020Break; Break
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN AUSTRALIA AS FOLLOWS: IT WAS REPORTED AN UNKNOWN DATE THAT THE OPEN RING CURETTE USED TO CLEAR OUT THE DISC MATERIAL IN AN ANTERIOR CERVICAL DISCECTOMY AND FUSION HAS SPLIT AND IS NOT ABLE TO USE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT DELAY. THERE WERE NO FRAGMENTS ARE GENERATED. THERE WERE NO PATIENT CONSEQUENCES. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9991458 ↗
Other CURETTE devices
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- Centurion 67600KCenturion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I67970Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion I68040Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 66745Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67050Centurion Medical Products Corporation · CURETTE1 recall0 reports
- Centurion 67430Centurion 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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