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Gemini M0063301110Recalls & reported problems

Boston Scientific Corporation · Paired Wire Helical Stone Retrieval Basket · Class 2

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 08714729043379), received between May 19, 2017 and May 19, 2017 — classified as 1 injury.

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

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 19, 2017Break; Break

    IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A GEMINI BASKET WAS USED FOR A URETEROSCOPY PROCEDURE IN THE URETER ON (B)(6) 2017. ACCORDING TO THE COMPLAINANT DURING THE PROCEDURE THE TIP OF THE BASKET DETACHED IN THE URETER. THE DETACHED PIECE WAS REMOVED FROM THE PATIENT. THE PROCEDURE WAS COMPLETED BY USING ANOTHER GEMINI BASKET. THERE WERE NO PATIENT COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. THE PATIENT'S CONDITION AT THE CONCLUSION OF THE PROCEDURE WAS REPORTED TO BE "FINE".

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6579944 ↗

Other DISLODGER, STONE, BASKET, URETERAL, METAL devices

All DISLODGER, STONE, BASKET, URETERAL, METAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.