NA 5140-533-625Recalls & reported problems
Stryker Leibinger GmbH & Co. KG · Needle Electrode GN, 15x1000mm · 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 07613327292107), received between Mar 27, 2019 and Mar 27, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Device Sensing Problem” (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
- Device Sensing Problem1
- Failure to Sense1
- Impedance Problem1
Patient problems
- Nerve Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 27, 2019Failure to Sense; Device Sensing Problem; Impedance Problem; Failure to Sense; Device Sensing Problem; Impedance Problem
IT WAS REPORTED THAT DURING A TOTAL THYROIDECTOMY PROCEDURE THE GROUND NEEDLE IMPEDANCE WAS INTERMITTENT, AND NERVE MONITORING FUNCTION WAS LOST. IT WAS REPORTED A VOCAL CORD NERVE WAS TRANSECTED, AND THE LEFT THYROIDECTOMY WAS NOT COMPLETED.
Patient problems: Nerve Damage
MAUDE report 8455038 ↗
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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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