MAUDE Adverse Event Report: ARGON MEDICAL DEVICES BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT 16GA X 10CM

Model Number	370-1080-02
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/04/2022
Type of Reportable Event	Malfunction
Event or Problem Description
Physician reports that this is a problem that is repeated in different procedures.In this case, during the use of the device, a lot of effort is required to fire the two triggers, and the patient is in danger of affecting sensitive structures near the biopsy site, with the danger of significant bleeding.In addition, in some cases after the effort of the shot, the samples obtained are broken or scarce.The hospital has lost confidence in the product and returns 38 unused units plus 2 double-bagged used units (one sterile unit); a total of 40 sample units from the same batch.Hospital needs a letter explaining the root cause of the incident and wacrees needs credit note per 40 units of the same reference.
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 this is a problem that is repeated in different procedures.In this case, during the use of the device, a lot of effort is required to fire the two triggers, and the patient is in danger of affecting sensitive structures near the biopsy site, with the danger of significant bleeding.In addition, in some cases after the effort of the shot, the samples obtained are broken or scarce.The hospital has lost confidence in the product and returns 38 unused units plus 2 double-bagged used units (one sterile unit); a total of 40 sample units from the same batch.Hospital needs a letter explaining the root cause of the incident and wacrees needs credit note per 40 units of the same reference.
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 this is a problem that is repeated in different procedures.In this case, during the use of the device, a lot of effort is required to fire the two triggers, and the patient is in danger of affecting sensitive structures near the biopsy site, with the danger of significant bleeding.In addition, in some cases after the effort of the shot, the samples obtained are broken or scarce.The hospital has lost confidence in the product and returns 38 unused units plus 2 double-bagged used units (one sterile unit); a total of 40 sample units from the same batch.Hospital needs a letter explaining the root cause of the incident and wacrees needs credit note per 40 units of the same reference.
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.One opened sample was returned by the customer.A functional inspection found that the trigger was hard to push and get the device to fire properly.The most likely cause of the hard triggers is friction between the catch and carriage components in the biopince device resulting in the need for excessive force to fire the device.Capa ca-00011 was initiated to fix this defect.Corrective actions are currently being worked on to reduce the amount of force needed to activate the triggers, at which time they will be implemented into the manufacturing process.The complaint is confirmed.

• Brand Name: BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT 16GA 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: 13968796
• Report Number: 0001625425-2022-00971
• Device Sequence Number: 5158850
• Product Code: KNW
• UDI-Device Identifier: 00886333224067
• UDI-Public: 00886333224067
• 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: User Facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 06/23/2022

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: 08/24/2024
• Device Model Number: 370-1080-02
• Device Catalogue Number: 370-1080-02
• Device Lot Number: 11383431
• 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: 03/24/2022
• Supplement Date Received by Manufacturer: 03/24/2022; 03/24/2022
• Initial Report FDA Received Date: 03/31/2022
• Supplement Report FDA Received Date: 05/03/2022; 06/23/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown