MAUDE Adverse Event Report: BECTON, DICKINSON AND COMPANY (BD) PAXGENE® BLOOD DNA TUBES; BLOOD/PLASMA COLLECTION DEVICE FOR DNA TESTING

Catalog Number	761165
Medical Device Problem Codes	Device Markings/Labelling Problem (2911); Inaccurate Information (4051)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/27/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A device evaluation is anticipated but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
Event or Problem Description
It was reported prior to using paxgene® blood dna tubes that 300 tubes had a tube label batch number different tan the shelf pack label.Additionally, there were a mix of two batch numbers within two shelf packs.There were no health impacts or consequences reported.
Additional Manufacturer Narrative
The following fields were updated due to additional information: d9: device available for evaluation: yes h.3 device eval by manufacturer? yes d9: returned to manufacturer on: 19-sep-2024 investigation summary material #: 761165 lot/batch #: 4095154 bd received 700 total samples (combined samples from (b)(6)) and 3 photos for investigation.The samples and photos were reviewed and the indicated failure mode for incorrect label information was observed.Evaluation of both indicated that the shelf label had a lot number 4095154 with expiry date 30th of april 2025, and tube labels of lot 4079048 with expiry date 31st of may 2025.Additionally, 200 retention samples from bd inventory, were evaluated by visual examination and upon completion the indicated failure mode for incorrect label information was not observed.Based on a review of the device history record for the incident lot, some product requirements for lot release were unmet and not discovered prior to release.There were no related quality issues during manufacturing of the product.This complaint has been confirmed for the indicated failure mode incorrect label information.A global hold has been placed on this batch number.Bd has initiated further root cause investigation relating to the issue of incorrect label information through situation analysis and corrective and preventive actions.Complaints received for this device and reported condition will continue to be tracked and trended.Our business team regularly reviews the collected data for identification of emerging trends.
Event or Problem Description
It was reported prior to using paxgene® blood dna tubes that 300 tubes had a tube label batch number different tan the shelf pack label.Additionally there were a mix of two batch numbers within two shelf packs.There were no health impacts or consequences reported.

• Brand Name: PAXGENE® BLOOD DNA TUBES
• Common Device Name: BLOOD/PLASMA COLLECTION DEVICE FOR DNA TESTING
• Manufacturer (Section D): BECTON, DICKINSON AND COMPANY (BD); belliver way; belliver industrial estate; plymouth ; UK
• Manufacturer (Section G): BECTON, DICKINSON AND COMPANY (BD); belliver way; belliver industrial estate; plymouth ; UK
• Manufacturer Contact: jo doyka ; 7 loveton circle; sparks, MD 21152 ; 4103164000
• MDR Report Key: 20353008
• Report Number: 9617032-2024-01591
• Device Sequence Number: 20819594
• Product Code: PJE
• UDI-Device Identifier: 04053727611659
• UDI-Public: (01)04053727611659(11)240404(17)250430(10)4095154
• Combination Product (Y/N): N
• Initial Reporter Country: BE
• PMA/510(K) Number: K231469
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/16/2024

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: Other
• Device Expiration Date: 04/30/2025
• Device Catalogue Number: 761165
• Device Lot Number: 4095154
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/02/2024
• Supplement Date Received by Manufacturer: 10/16/2024
• Initial Report FDA Received Date: 10/02/2024
• Supplement Report FDA Received Date: 10/22/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/04/2024
• 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
• Patient Sex: Unknown