MAUDE Adverse Event Report: BARD PERIPHERAL VASCULAR, INC. TREK BONE LESION BIOPSY KIT; BIOPSY INSTRUMENT

Catalog Number TKL1110

Device Problems Material Perforation (2205); Device Contamination with Chemical or Other Material (2944); Unintended Movement (3026); Premature Separation (4045)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 08/22/2023

Event Type  malfunction  

Event Description

It was reported that during a bone lesion biopsy in the sclerotic bone, the needle allegdly wobbled.It was further that the procedure was then stopped, and upon release of the needle it was noted that the quick connect had become completely disconnected from the drill.The procedure was completed using another device.There was no reported patient injury.

Manufacturer Narrative

H10: as the lot number for the device was provided, a review of the device history records is currently being performed.The device has been returned to the manufacturer for evaluation.The investigation of the reported event is currently underway.H10: d4 (expiration date: 01/2024).H11: section a through f ¿ the information provided by bd represents all the known information at this time.Despite good faith efforts to obtain additional information, the complainant/reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.

Event Description

It was reported that during a bone lesion biopsy in the sclerotic bone, the needle allegedly wobbled.It was further reported that the procedure was then stopped, and upon release of the needle it was noted that the quick connect had become completely disconnected from the drill.The procedure was completed using another device.There was no reported patient injury.

Manufacturer Narrative

H10: manufacturing review: the device history records have been reviewed and this lot met all release criteria.There was nothing found to indicate there was a manufacturing related cause for this event.Investigation summary: one quick connect hub and sterile sleeves were received for evaluation.During visual evaluation, a tear was noted to the sleeve and it was also noted when the device was viewed under the microscope, the proximal uclips were not visible and black residue was noted on the inner side of the quick connect hub.No other visual anomalies were noted to the device.Further functional testing was not performed due to the condition the sample was received.Therefore, the investigation is confirmed for the reported unintended movement and premature separation issue as uclips were not visible which causes the wobble on the quick connect hub, the investigation is also confirmed for the identified material perforation as a tear was noted on the sterile sleeve and the investigation is confirmed for the identified device contamination with chemical or other material as black residue was noted to the device.A definitive root cause for the alleged unintended movement and premature separation issues were due to the missing of uclips (e.G., not visible).Then, definitive root cause for the identified material perforation and identified device contamination with chemical or other material issues could not be determined based upon the provided information.Labeling review: as the reported event did not allege a labeling or use related issue, a labeling review is not required.H10: d4 (expiration date: 01/2024), g3, h6 (method) h11: e1, h6 (result, conclusion) h11: section a through f ¿ the information provided by bd represents all the known information at this time.Despite good faith efforts to obtain additional information, the complainant/reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.H3 other text : see h10.

• Brand Name: TREK BONE LESION BIOPSY KIT
• Type of Device: BIOPSY INSTRUMENT
• Manufacturer (Section D): BARD PERIPHERAL VASCULAR, INC.; 1625 w 3rd st.; tempe AZ 85281
• Manufacturer (Section G): CAREFUSION MANNFORD; 400 foster rd; mannford OK 74044
• Manufacturer Contact: brett curtice ; 800 w. rio salado pkwy; tempe, AZ 85281 ; 4803032689
• MDR Report Key: 18722306
• MDR Text Key: 335716986
• Report Number: 2020394-2024-00215
• Device Sequence Number: 1
• Product Code: KNW
• UDI-Device Identifier: 00801741201455
• UDI-Public: (01)00801741201455
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K213896
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Health Professional,User Facility,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 03/07/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/16/2024
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: TKL1110
• Device Lot Number: 0001507177
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/21/2023
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 03/07/2024
• Was Device Evaluated by Manufacturer?: Yes
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Sex: Female