MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION INTERJECT; BIOPSY NEEDLE KIT

Model Number	M00518301
Medical Device Problem Code	Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/02/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Initial reporter address 1: (b)(6).The device has been received for analysis; however, the analysis has not yet been completed.Upon completion of the failure analysis of the complaint device, if there is any further relevant information from that review, a supplemental medwatch will be filed.
Event or Problem Description
It was reported to boston scientific corporation that an interject needle was used in the small intestine during a colonoscopy procedure performed on (b)(6) 2021.During the procedure, the needle detached in two pieces.The device was removed from the patient and the procedure was completed with another interject needle.There were no patient complications reported as a result of this event.The patient's condition at the conclusion of the procedure was reported to be stable.
Event or Problem Description
It was reported to boston scientific corporation that an interject needle was used in the small intestine during a colonoscopy procedure performed on (b)(6) 2021.During the procedure, the needle detached in two pieces.The device was removed from the patient and the procedure was completed with another interject needle.There were no patient complications reported as a result of this event.The patient's condition at the conclusion of the procedure was reported to be stable.
Additional Manufacturer Narrative
Block e1: initial reporter address 1: (b)(6).Block h6: medical device problem code a0501 captures the reportable event of needle detached.The returned interject needle was analyzed, a visual evaluation was performed which noted that the inner hub separated from the outer hub.The needle was exposed and it was confirmed that it was not broken, it was properly attached to the device.Marks in the inner hub were visible on the device indicating the locking feature for the inner hub was used.Additionally, marks were observed in the outer hub indicating that the components were previously joined.No other issues noted.Based on all available information, it is possible that handling and manipulation of the device during unpacking/prepping/testing or during the use of the device could have contributed to the handle detaching.Therefore, the most probable root cause for the problem found during the analysis is adverse event related to procedure.However, the reported issue of needle detached was not confirmed during the analysis.This device met all manufacturing requirements and no abnormalities were reported during the manufacturing process; after analysis it was determined that the needle was not broken, it was properly attached to the device.Therefore, the root cause for the reported failure is no problem detected.A review of the manufacturing documentation for this device revealed that no anomalies or deviations related to the event occurred during manufacturing.

• Brand Name: INTERJECT
• Common Device Name: BIOPSY NEEDLE KIT
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• MDR Report Key: 11592589
• Report Number: 3005099803-2021-01268
• Device Sequence Number: 11957417
• Product Code: FCG
• UDI-Device Identifier: 08714729296508
• UDI-Public: 08714729296508
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K171454
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,distri
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/23/2021

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: 07/29/2023
• Device Model Number: M00518301
• Device Catalogue Number: 1830
• Device Lot Number: 0025784239
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/22/2021
• Initial Date Received by Manufacturer: 03/05/2021
• Supplement Date Received by Manufacturer: 03/31/2021
• Initial Report FDA Received Date: 03/30/2021
• Supplement Report FDA Received Date: 04/23/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 69 YR