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Expand 212® Helical Stone Basket with Filiform Tip 041490Recalls & reported problems

C. R. Bard, Inc. · Expand 212® Helical Stone Basket with Filiform Tip · 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 00801741076480), received between Jun 23, 2023 and Jun 23, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Nonstandard Device” (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.

Most reported problems

Device problems

  • Nonstandard Device1

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.

  • MalfunctionJun 23, 2023Nonstandard Device; Nonstandard Device

    IT WAS REPORTED THAT A PHYSICIAN STATED IN AN ONLINE SURVEY THAT THEY WERE NOT ABLE TO SUCCESSFULLY REMOVE THE URETERAL STONE WHILE USING AN EXPAND STONE BASKET BECAUSE THE STONE WAS VERY LARGE AND RESIDUAL CONCRETIONS REMAINED IN SITU.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17192109 ↗

Other DISLODGER, STONE, BASKET, URETERAL, METAL devices

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

Sources and updates

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