Endoflip EF-302Recalls & reported problems
Covidien LP · 300 Display System With Reader · Class 2
Data updated Oct 13, 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 10884521826816), received between Mar 19, 2025 and Mar 19, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Sparking” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Sparking1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 19, 2025Sparking; Sparking
IT WAS REPORTED THAT WHEN THE CORD WAS PLUGGED IN, IT SEEMED THAT THERE WAS A CRACKED. THE CUSTOMER STATED THAT THEY HAVE SEEN SPARKS COME FROM THE AREA. THERE WAS NO PATIENT INVOLVEMENT.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 21648533 ↗
Other SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL) devices
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- Solar GI LGI H20, Trolley system G3-6Medical Measurement Systems B.V. · SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)1 recall3 reports
- Solar GI HRM H20, 24p, Trolley system G3-8Medical Measurement Systems B.V. · SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)1 recall2 reports
- Solar GI HRM H2O, 36p, Trolley system G3-12Medical Measurement Systems B.V. · SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)1 recall1 report
- EndoFLIP EF-100Covidien LP · System, Gastrointestinal Motility (Electrical)1 recall0 reports
- Solar GI HRM H20, 24p, Compact Pole system G3-7Medical Measurement Systems B.V. · SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)1 recall0 reports
- Zvu® ZVU-3Diversatek Healthcare, Inc. · System, Gastrointestinal Motility (Electrical)1 recall0 reports
- Endoflip RFG-EF100Covidien LP · SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)1 recall0 reports
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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