MAUDE Adverse Event Report: ARGON MEDICAL DEVICES BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT 18GA X 10CM

Model Number	360-1080-02
Medical Device Problem Code	Firing Problem (4011)
Health Effect - Clinical Codes	Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/26/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The sample is indicated as available for return.As of the date of this report, the sample has not been returned.A follow-up report will be provided once the device has been received and reviewed.
Event or Problem Description
Physician reports that during a procedure with 1 unit; in a first attempt to shoot, this does not occur.However, a few seconds later, he shoots himself without any medical supervision.The doctors classified what happened as serious, since it puts the integrity of the patient at risk.The hospital returns the used unit in a double bag, for review at argon.They need a letter explaining the root cause of the incident.
Additional Manufacturer Narrative
The sample is indicated as returned.As of the date of this report, the sample has not been evaluated.A follow-up report will be provided once the device has been reviewed.
Event or Problem Description
Physician reports that during a procedure with 1 unit; in a first attempt to shoot, this does not occur.However, a few seconds later, he shoots himself without any medical supervision.The doctors classified what happened as serious, since it puts the integrity of the patient at risk.The hospital returns the used unit in a double bag, for review at argon.They need a letter explaining the root cause of the incident.
Additional Manufacturer Narrative
A review of the dhrs of the top level and sublots as well as the inspection records was conducted, and no deviations or non-conformances were found relating to this issue.Three opened sample were returned from the customer for review.A visual inspection was performed on the returned products.Two devices fired perfectly fine in all three stroke lengths from front and rear trigger without any delays.One device's front carriage ramp was having some kind of deformation.The complaint is confirmed for one device.This might have happened when the device is being fired in locked state causing damage to the front carriage ramp portion.No corrective action can be taken at this time as this issue is an isolated one.
Event or Problem Description
Physician reports that during a procedure with 1 unit; in a first attempt to shoot, this does not occur.However, a few seconds later, the device shoots without any medical supervision.

• Brand Name: BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT 18GA X 10CM
• Common Device Name: BIOPINCE
• Manufacturer (Section D): ARGON MEDICAL DEVICES; 1445 flat creek rd; athens TX 75751
• Manufacturer Contact: elnaz rahman ; 1445 flat creek rd; athens, TX 75751 ; 9036759321
• MDR Report Key: 16458290
• Report Number: 0001625425-2023-00983
• Device Sequence Number: 2315913
• Product Code: KNW
• UDI-Device Identifier: 00886333224005
• UDI-Public: 00886333224005
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K904987
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/12/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 06/15/2025
• Device Model Number: 360-1080-02
• Device Catalogue Number: 360-1080-02
• Device Lot Number: 11426491
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/21/2023
• Supplement Date Received by Manufacturer: 02/21/2023; 02/21/2023
• Initial Report FDA Received Date: 03/01/2023
• Supplement Report FDA Received Date: 04/06/2023; 05/12/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/15/2022
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown