NA 0504881314Recalls & reported problems
Stryker Corporation · [Cutting Loop Electrode, .014 wire, 27 Fr ¿ 90 ¿, Only for use with Stryker Resectoscopes 0502-880-401, 0502-880-402, Do not use if package is damaged] · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327055511), received between Nov 16, 2020 and Nov 16, 2020 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (4 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 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component4
- Electrical Power Problem4
Patient problems
- Insufficient Information4
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 16, 2020Electrical Power Problem; Detachment of Device or Device Component; Electrical Power Problem
IT WAS REPORTED THAT THE CUTTING LOOP DETACHED FROM THE PROBE. THE DETACHED PIECE WAS RETRIEVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 10847495 ↗MalfunctionNov 16, 2020Electrical Power Problem; Detachment of Device or Device Component; Electrical Power Problem
IT WAS REPORTED THAT THE CUTTING LOOP DETACHED FROM THE PROBE. THE DETACHED PIECE WAS RETRIEVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 10847424 ↗MalfunctionNov 16, 2020Electrical Power Problem; Detachment of Device or Device Component; Electrical Power Problem
IT WAS REPORTED THAT THE CUTTING LOOP DETACHED FROM THE PROBE. THE DETACHED PIECE WAS RETRIEVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 10847383 ↗MalfunctionNov 16, 2020Electrical Power Problem; Detachment of Device or Device Component; Electrical Power Problem
IT WAS REPORTED THAT THE CUTTING LOOP DETACHED FROM THE PROBE. THE DETACHED PIECE WAS RETRIEVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 10847372 ↗
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- OES CYSTONEPHROFIBERSCOPE OLYMPUS CYF-5ROlympus Medical Systems Corp. · Cystoscope and accessories, flexible/rigid114 reports
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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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