Jawz Endomyocardial Biopsy Forcep 190095Recalls & reported problems
Argon Medical Devices, Inc. · Jawz Endomyocardial Biopsy Forceps 5F x 105cm Straight · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00886333206865), received between May 1, 2024 and May 1, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 1, 2024Break; Break
THE REPORTER INDICATED THE DEVICE WILL NOT OPEN OR CLOSE. ADDITIONAL INFORMATION WAS REQUESTED AND RECEIVED INDICATING THE PATIENT NEEDED SURGICAL EXPLORATION OF THE GROIN TO RETRIEVE THE BROKEN DEVICE INSIDE THE FEMORAL VEIN, FOLLOWED BY SURGICAL REPAIR OF THE FEMORAL VEIN. THE INTENDED PROCEDURE WAS ABANDONED.
Patient problems: Insufficient Information
MAUDE report 19221234 ↗
Other Device, Biopsy, Endomyocardial devices
- Biopsy Forceps 504300Cordis US Corp. · DEVICE, BIOPSY, ENDOMYOCARDIAL3 reports
- Cook G05389Cook Incorporated · DEVICE, BIOPSY, ENDOMYOCARDIAL3 reports
- Jawz Endomyocardial Biopsy Forceps 190075Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial3 reports
- Biopsy Forceps 504302Cordis Corporation · DEVICE, BIOPSY, ENDOMYOCARDIAL2 reports
- Jawz Endomyocardial Biopsy Forceps 190070Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial2 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
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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