GAS TUBE MA-238Recalls & reported problems
Olympus Medical Systems Corp. · MA-238 GAS CONNECTING TUBE F/ CF-MB2/LB2 · Class 2
Data updated Oct 18, 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 04953170064517), received between May 2, 2025 and May 2, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Explosion” (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.
Reports received per month
Most reported problems
Device problems
- Explosion1
Patient problems
- 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.
MalfunctionMay 2, 2025Explosion; Explosion
NO ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21952058 ↗
Other Choledochoscope and accessories, flexible/rigid devices
- SpyScope DS M00546600Boston Scientific Corporation · Choledochoscope and accessories, flexible/rigid912 reports
- SpyScope™ DS II M00546610Boston Scientific Corporation · Choledochoscope and accessories, flexible/rigid2 deaths646 reports
- Forceps/Irrigation Plug (Isolated Type) MAJ-891Olympus Medical Systems Corp. · Choledochoscope and accessories, flexible/rigid1 recall1 death257 reports
- OES CHOLEDOCHOFIBERSCOPE OLYMPUS CHF TYPE CB30LOlympus Medical Systems Corp. · Choledochoscope and accessories, flexible/rigid1 recall9 reports
- SpyGlass™ Discover M00546780Boston Scientific Corporation · Choledochoscope and accessories, flexible/rigid1 death55 reports
- Tangent Digital catheter tng-4002-indTangent Endoscopy LLC · Choledochoscope And Accessories, Flexible/Rigid1 recall0 reports
- OES TRANSDUODENAL CHOLEDOCHOFIBERSCOPE OLYMPUS CHF TYPE BP30Olympus Medical Systems Corp. · Choledochoscope and accessories, flexible/rigid1 recall0 reports
- SpyGlass DS M0054665R0Boston Scientific Corporation · Choledochoscope and accessories, flexible/rigid19 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 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.
How reports and recalls are matched · Editorial policy · Report an error on this page