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Single Use Retrieval Basket V FG-V421PRRecalls & reported problems

Olympus Medical Systems Corp. · Single Use Retrieval Basket V · Class 2

All models of Single Use Retrieval Basket V (4)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
4
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04953170244032), received between Oct 3, 2018 and May 21, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Obstruction of Flow” (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 18, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 2 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Obstruction of Flow2
  • Adverse Event Without Identified Device or Use Problem1
  • Break1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • No Code Available2

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 21, 2025Obstruction of Flow; Obstruction of Flow

    IT WAS REPORTED DURING SEDATION OF A THERAPEUTIC LARGE STONE REMOVAL THE BASKET WAS STUCK IN THE COMMON BILE DUCT AND THE BASKET ENVELOPED THE STONE, WIRES /SHEATH TWISTED, WIRES HAD TO BE CUT, GI DOC DILATED THE COMMON BILE DUCT MULTIPLE TIMES, UNTIL FINALLY STONE WAS RELEASED 2 HOURS LATER RESULTING IN A PROCEDURAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22063560 ↗
  • InjuryMay 21, 2025Obstruction of Flow; Obstruction of Flow

    IT WAS REPORTED DURING SEDATION OF A THERAPEUTIC LARGE STONE REMOVAL THE BASKET WAS STUCK IN THE COMMON BILE DUCT AND THE BASKET ENVELOPED THE STONE, WIRES /SHEATH TWISTED, WIRES HAD TO BE CUT, GI DOC DILATED THE COMMON BILE DUCT MULTIPLE TIMES, UNTIL FINALLY STONE WAS RELEASED 2 HOURS LATER RESULTING IN A PROCEDURAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22063541 ↗
  • InjuryJul 20, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    OLYMPUS MEDICAL SYSTEMS CORP. (OMSC) RECEIVED A LITERATURE TITLE "COMPARISON BETWEEN ENDOSCOPIC TREATMENT AND SURGICAL DRAINAGE OF THE PANCREATIC DUCT IN CHRONIC PANCREATITIS". THE LITERATURE REPORTED THE RESULTS OF A STUDY BASED ON THE ENDOSCOPIC OR SURGICAL DRAINAGE OF 51 PATIENTS WITH CHRONIC PANCREATITIS BETWEEN 2001 AND 2010. DURING THE STUDY PERIOD, LITHECTOMY WERE PERFORMED WITH THE USE OF OLYMPUS RETRIEVAL BASKET, AND BASKET IMPACTION OCCURRED IN 1 PATIENT. THERE IS NO DESCRIPTION ABOUT THE RELATIONSHIP BETWEEN OLYMPUS PRODUCT AND ADVERSE EVENT.

    Patient problems: No Code Available

    MAUDE report 10299575 ↗
  • InjuryOct 3, 2018Break; Break

    DURING A REMOVAL OF CALCULUS, THE SUBJECT DEVICE WAS USED. IN THE PROCEDURE, THE BASKET WIRE WAS INCARCERATED. THE PHYSICIAN TRIED TO CRUSH THE CALCULUS WITH THE EMERGENCY HANDLE, BUT THE BASKET WIRE BROKE. THE PATIENT WAS SENT TO OPEN SURGERY AND THE FRAGMENT WAS REMOVED. NO FURTHER INFORMATION WAS PROVIDED.

    Patient problems: No Code Available

    MAUDE report 7929087 ↗

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Sources and updates

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