Bard® Platinum Class™ Non-Retracting Grasping Forceps 039690Recalls & reported problems
C. R. Bard, Inc. · Bard® Platinum Class™ Non-Retracting Grasping Forceps · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741076558), received between Oct 27, 2020 and Oct 30, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Fragmentation” (3 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.
Most reported problems
Device problems
- Material Fragmentation3
- Device Handling Problem2
- Misassembly by Users1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Consequences Or Impact To Patient2
- No Patient Involvement2
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 30, 2020Material Fragmentation; Device Handling Problem; Material Fragmentation; Device Handling Problem
IT WAS REPORTED THAT ONE DORMIA PROBE WAS FOUND TO BE BROKEN WHEN THE BOX WAS OPENED AND THE BASKET ROD WAS NOT ATTACHED TO THE HANDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Patient Involvement
MAUDE report 10766624 ↗MalfunctionOct 29, 2020Material Fragmentation; Device Handling Problem; Material Fragmentation; Device Handling Problem
IT WAS REPORTED THAT ONE DORMIA PROBE BROKEN WHEN THE BOX WAS OPENED AND BASKET ROD NOT ATTACHED TO THE HANDLE. FOR THE SECOND PROBE, THE ROD HAD DETACHED FROM THE HANDLE AFTER A SINGLE USE AND WITHOUT EVEN FORCING IT. BOTH WERE FROM THE SAME LOT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient
MAUDE report 10755764 ↗MalfunctionOct 27, 2020Material Fragmentation; Misassembly by Users; Material Fragmentation; Misassembly by Users
IT WAS REPORTED THAT ONE DORMIA PROBE BROKEN WHEN THE BOX WAS OPENED AND BASKET ROD NOT ATTACHED TO THE HANDLE. FOR THE SECOND PROBE, THE ROD HAD DETACHED FROM THE HANDLE AFTER A SINGLE USE AND WITHOUT EVEN FORCING IT. BOTH WERE FROM THE SAME LOT.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Consequences Or Impact To Patient; No Patient Involvement
MAUDE report 10740381 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page