Crossfire 0475000100Recalls & reported problems
Stryker Corporation · Footswitch · Class 2
All models of Crossfire (3)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613327058093), received between Dec 16, 2022 and Aug 2, 2023 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Continuous Firing” (2 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
- Continuous Firing2
- Temperature Problem2
- Device Emits Odor1
- Electrical Shorting1
- Smoking1
- Thermal Decomposition of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
- Insufficient Information2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 2, 2023Continuous Firing; Continuous Firing
IT WAS REPORTED THAT THE DEVICE CAUSED CONTINUOUS ACTIVATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17446684 ↗MalfunctionAug 2, 2023Continuous Firing; Continuous Firing
IT WAS REPORTED THAT THE DEVICE CAUSED CONTINUOUS ACTIVATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17446569 ↗MalfunctionJun 7, 2023Electrical Shorting; Electrical Shorting
IT WAS REPORTED THAT THERE WAS A THERMAL EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17083379 ↗MalfunctionDec 21, 2022Temperature Problem; Thermal Decomposition of Device; Temperature Problem
IT WAS REPORTED THAT THERE WAS A THERMAL EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16030284 ↗MalfunctionDec 21, 2022Smoking; Smoking
IT WAS REPORTED THAT THERE WAS A THERMAL EVENT.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16023959 ↗MalfunctionDec 16, 2022Device Emits Odor; Temperature Problem
IT WAS REPORTED THAT THERE WAS A THERMAL EVENT FOR BURNING SMELL.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16000006 ↗
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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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