SpyGlass™ Discover M00542990Recalls & reported problems
Boston Scientific Corporation · SpyGlass™ Discover Retrieval Basket · Class 2
All models of SpyGlass Discover (4)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00191506004255), received between Feb 7, 2025 and Feb 7, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Difficult to Open or Close” (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
- Difficult to Open or Close1
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.
InjuryFeb 7, 2025Difficult to Open or Close; Difficult to Open or Close
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A SPYGLASS DISCOVER WAS USED IN THE CYSTIC DUCT DURING A LAPAROSCOPIC COMMON BILE DUCT EXPLORATION (LCBDE) DISCOVER PROCEDURE PERFORMED ON (B)(6) 2025. DURING PROCEDURE, A DISCOVER BASKET WAS USED WITH A SPYCOPE TO ATTEMPT TO REMOVE A STONE. HOWEVER, THE STONE WAS TOO LARGE TO BE REMOVE FROM THE DUCT AND GOT STUCK INSIDE THE BASKET. THERE WERE NO VISIBLE DAMAGE NOTED ON THE BASKET. THE PATIENT WAS THEN CONVERTED TO OPEN SURGERY. THE BASKET WAS DISASSEMBLED TO REMOVE THE SCOPE OFF. THE STONE WAS SUCCESSFULLY REMOVED FROM THE BASKET. THE BASKET AND STONE WAS SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21335233 ↗
Other DISLODGER, STONE, BILIARY devices
- Memory Basket G25149Cook Incorporated · DISLODGER, STONE, BILIARY75 reports
- Stonetome M00535110Boston Scientific Corporation · DISLODGER, STONE, BILIARY74 reports
- Stonetome M00535150Boston Scientific Corporation · DISLODGER, STONE, BILIARY67 reports
- Cook G36250Cook Incorporated · DISLODGER, STONE, BILIARY1 recall10 reports
- NCompass G36251Cook Incorporated · DISLODGER, STONE, BILIARY1 recall8 reports
- Strange G09108Cook Incorporated · DISLODGER, STONE, BILIARY1 recall1 report
- Single Use Retrieval Nitinol Basket V FG-V451POlympus Medical Systems Corp. · DISLODGER, STONE, BILIARY31 reports
- SpyGlass™ Retrieval Basket M00546550Boston Scientific Corporation · DISLODGER, STONE, BILIARY23 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.
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