NA 702497Recalls & reported problems
Stryker GmbH · Extractor · Class 1
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 04546540112422), received between Jan 2, 2019 and Jan 2, 2019 — 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
- Difficult to Remove1
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.
MalfunctionJan 2, 2019Break; Difficult to Remove
THE DOCTOR CONFIRMED THAT BONE UNION, SO DEPLOYED TWO ASSNIS 4.0 SCREWS WERE TRIED TO REMOVE WITH EXTRACTOR. HOWEVER THESE WERE NOT ABLE TO BE REMOVED AND THE TIP OF THE EXTRACTOR WAS BROKEN AND LEFT IN THE PATIENT BODY. THE TIP OF THE EXTRACTOR WAS LEFT IN THE PATIENT BODY. THE SCREWS WERE NOT REMOVED.
Patient problems: Foreign Body In Patient
MAUDE report 8210625 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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