OSTYCUT® 17860070Recalls & reported problems
Angiomed GmbH & Co. Medizintechnik KG · OSTYCUT® Disposable Bone Biopsy Needles, 14.5g x 150mm · Class 1
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 00801741083792), received between May 25, 2018 and May 25, 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
- Fracture1
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.
MalfunctionMay 25, 2018Break; Fracture; Break; Fracture
IT WAS REPORTED THAT APPROXIMATELY TWO MILLIMETERS OF THE BEVELED NEEDLE TIP ALLEGEDLY FRACTURED WITHIN THE PATIENT AS THE DEVICE WAS BEING REMOVED. THIS OCCURRED DURING A CT-GUIDED RIB BIOPSY. IT WAS FURTHER REPORTED THAT THERE WAS NO ATTEMPT TO RETRIEVE THE DETACHED TIP. THE BONE SAMPLE WAS OBTAINED AND THE PROCEDURE WAS COMPLETED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7546044 ↗
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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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