Bard® Dimension® Stone Basket 042310Recalls & reported problems
C. R. Bard, Inc. · Bard® Dimension® Stone Basket · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741066801), received between May 23, 2018 and Sep 7, 2018 — classified as 2 malfunctions.
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.
Most reported problems
Device problems
- Difficult to Open or Close1
- Difficult to Remove1
- Material Twisted/Bent1
- Mechanical Jam1
Patient problems
- No Consequences Or Impact To Patient2
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 7, 2018Material Twisted/Bent; Material Twisted/Bent
IT WAS REPORTED THAT THE BASKET DID NOT CLOSE COMPLETELY. PER ADDITIONAL INFORMATION: ON (B)(6), DR. (B)(6), A UROLOGIST AT THE (B)(6) CLINIC, WAS DOING A FLEXIBLE URETEROSCOPY AND WHILE CAPTURING THE CALCULUS WITH THE DIMENSION BASKET FROM BARD; IT DID NOT COMPLETELY CLOSE, WHICH PREVENTED IT FROM BEING SAFELY REMOVED FROM THE PATIENT. THERE WAS A DELAY IN THE PROCEDURE DURING REMOVAL OF THE BASKET AND ADDITIONAL SURGICAL TIME. THE DOCTOR WAS ABLE TO FRAGMENT AND SAFELY REMOVE THE DEVICE FROM THE PATIENT. IT WAS LATER NOTED ON 13 AUG 2018 THE SHAFT OF THE DEVICE WAS SEVERELY BENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7855569 ↗MalfunctionMay 23, 2018Difficult to Remove; Difficult to Open or Close; Mechanical Jam; Difficult to Open or Close
IT WAS REPORTED THAT THE BASKET DID NOT CLOSE COMPLETELY. THE UROLOGIST WAS PERFORMING A FLEXIBLE URETEROSCOPY. DURING CAPTURE OF THE CALCULUS, THE DIMENSION BASKET DID NOT CLOSE COMPLETELY WHICH PREVENTED IT FROM BEING SAFELY REMOVED FROM THE PATIENT. THERE WAS A DELAY IN THE PROCEDURE AND ADDITIONAL SURGICAL TIME TO REMOVE THE BASKET. THE DOCTOR WAS ABLE TO FRAGMENT IT AND REMOVE IT SAFELY FROM THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 7539288 ↗
Other DISLODGER, STONE, BASKET, URETERAL, METAL devices
- Zero Tip M0063901050Boston Scientific Corporation · DISLODGER, STONE, BASKET, URETERAL, METAL287 reports
- NCircle G18778Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL226 reports
- NCircle G46206Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL197 reports
- NCircle G17520Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL129 reports
- NGage G48297Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL96 reports
- NGage G48294Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL92 reports
- NCircle G19110Cook Incorporated · DISLODGER, STONE, BASKET, URETERAL, METAL88 reports
- Bard® SkyLite™ Tipless Nitinol Stone Basket 041900C. R. Bard, Inc. · DISLODGER, STONE, BASKET, URETERAL, METAL78 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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