Wittich G07313Recalls & reported problems
Cook Incorporated · Wittich Nitinol Stone Basket · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00827002073135), received between Sep 5, 2018 and Feb 1, 2023 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break2
- Material Separation1
Patient problems
- Foreign Body In Patient1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryFeb 1, 2023Material Separation; Material Separation
NO ADDITIONAL INFORMATION REGARDING PATIENT AND/OR EVENT DETAILS HAS BEEN RECEIVED SINCE THE PREVIOUS MEDWATCH REPORT WAS SENT.
Patient problems: Foreign Body In Patient
MAUDE report 16280742 ↗MalfunctionOct 29, 2018Break; Break
IT WAS REPORTED A WITTICH NITINOL STONE BASKET WAS USED FOR AN UNSPECIFIED STONE REMOVAL PROCEDURE. DURING THE PROCEDURE THE MIDDLE OF THE BASKET WIRE WAS BROKEN. THE PHYSICIAN USED A NEW PRODUCT TO COMPLETE THE PROCEDURE. AS REPORTED, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS OR REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8015964 ↗MalfunctionSep 5, 2018Break; Break
IT WAS REPORTED A WITTICH NITINOL STONE BASKET BROKE DURING AN UNSPECIFIED PROCEDURE. ADDITIONAL EVENT DETAILS HAVE NOT BEEN RECEIVED AT THIS TIME. AS REPORTED, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS OR REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7847839 ↗
Other DISLODGER, STONE, BILIARY devices
- Memory Basket G25149Cook Incorporated · DISLODGER, STONE, BILIARY75 reports
- Stonetome M00535110Boston Scientific Corporation · DISLODGER, STONE, BILIARY74 reports
- Stonetome M00535150Boston Scientific Corporation · DISLODGER, STONE, BILIARY67 reports
- Cook G36250Cook Incorporated · DISLODGER, STONE, BILIARY1 recall10 reports
- NCompass G36251Cook Incorporated · DISLODGER, STONE, BILIARY1 recall8 reports
- Strange G09108Cook Incorporated · DISLODGER, STONE, BILIARY1 recall1 report
- Single Use Retrieval Nitinol Basket V FG-V451POlympus Medical Systems Corp. · DISLODGER, STONE, BILIARY31 reports
- SpyGlass™ Retrieval Basket M00546550Boston Scientific Corporation · DISLODGER, STONE, BILIARY23 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.