Procure™ 408296Recalls & reported problems
St. Jude Medical, Inc. · Endomyocardial Biopsy Forceps · Class 2
Data updated Oct 13, 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 05415067009548), received between Aug 1, 2018 and Aug 1, 2018 — classified as 1 malfunction.
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Difficult to Open or Close1
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.
MalfunctionAug 1, 2018Difficult to Open or Close
ENDOMYOCARDIAL BIOPSY FORCEPS DID NOT OPEN PROPERLY DURING BIOPSY PROCEDURE, REQUIRING A NEW FORCEPS TO BE USED. NO HARM TO THE PT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7742740 ↗
Other DEVICE, BIOPSY, ENDOMYOCARDIAL devices
- Jawz Endomyocardial Biopsy Forceps 190075Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial3 reports
- Cook G05389Cook Incorporated · DEVICE, BIOPSY, ENDOMYOCARDIAL3 reports
- Biopsy Forceps 504300Cordis US Corp. · DEVICE, BIOPSY, ENDOMYOCARDIAL3 reports
- Jawz Endomyocardial Biopsy Forceps 190081Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial2 reports
- Jawz Endomyocardial Biopsy Forceps 190051Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial2 reports
- Jawz Endomyocardial Biopsy Forceps 190030Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial2 reports
- Jawz Endomyocardial Biopsy Forceps 190070Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial2 reports
- Biopsy Forceps 504302Cordis Corporation · DEVICE, BIOPSY, ENDOMYOCARDIAL2 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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