CONMED 149RRecalls & reported problems
Conmed Corporation · CONMED DISPOSABLE BRONCHIAL CYTOLOGY BRUSH, Ring Handle, 3 mm X 120 cm · Class 2
- 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 10653405052401), received between May 17, 2016 and May 17, 2016 — 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break1
- Component Falling1
- Detachment Of Device Component1
Patient problems
- Foreign Body In Patient1
- Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 17, 2016Break; Detachment Of Device Component; Component Falling
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- superDimension AKI00100-01Covidien LP · endoscopic cytology brush5 reports
- Infinity 00711652US Endoscopy · endoscopic cytology brush4 reports
- CytoMax II G22674Cook Incorporated · endoscopic cytology brush4 reports
- superDimension SDNB2000Covidien LP · endoscopic cytology brush1 death3 reports
- Hobbs Microbiology Brush 4310Hobbs Medical, Inc. · Endoscopic Cytology Brush2 reports
- Infinity 00711499US Endoscopy · endoscopic cytology brush2 reports
- Infinity 00711653US Endoscopy · endoscopic cytology brush2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.