Jawz Endomyocardial Biopsy Forcep 190065Recalls & reported problems
Argon Medical Devices, Inc. · Jawz Endomyocardial Biopsy Forceps 6F x 50cm Straight · Class 2
Data updated Oct 18, 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 00886333206773), received between Sep 19, 2022 and Sep 19, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 19, 2022Physical Resistance/Sticking
DURING PROCEDURE, A PHYSICIAN STOPPED USING THE JAWS AS THE JAWS ACTION(OPEN/CLOSE) WAS SLOW IN RESPONSE TO THE MANIPULATION. THE JAWS WAS REPLACED WITH AN ADDITIONALLY OPENED 190065, AND THE PROCEDURE WAS COMPLETED. AS A RESULT OF THE RETURNED SAMPLE(S) REVIEW AT GMKK: THE JAWS ACTION(OPEN/CLOSE) WAS SLOW RESPONSE WITH SOME RESISTANCE, WHEN IT WAS IN CURVED SITUATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15445742 ↗
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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