MAUDE Adverse Event Report: BECTON DICKINSON PROTECTOR P21; CLOSED ANTINEOPLASTIC AND HAZARDOUS DRUG RECONSTITUTION AND TRANSFER SYSTEM

Catalog Number	515102
Medical Device Problem Code	Leak/Splash (1354)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	11/12/2024
Type of Reportable Event	Malfunction
Event or Problem Description
The product leaks during use.
Additional Manufacturer Narrative
Initial mdr submission.A follow up mdr will be submitted if additional information, a device evaluation, or a device history review is completed.
Additional Manufacturer Narrative
D tab updated.Catalog and lot number correction.
Event or Problem Description
Additional information: 19feb2025: yes, customer confirmed that a mistake was made from their side and it should be sku 515102 on (b)(4).
Additional Manufacturer Narrative
(b)(4) follow up mdr for device evaluation: one used and one unused sample was provided to our quality team for investigation.Through visual inspection, no damage or other defects were observed on either device.The used protector was verified to be properly assembled onto the vial.Functional testing was completed, liquid was observed within the expansion chamber, however, no leakage was noted between the protector and vial.The protector was removed for further evaluation and the stopper of the vial was noted to have multiple puncture marks along the metal cap.A device history review was performed for reported lot 2404132, no deviations or non-conformances were identified during the manufacturing process that could have contributed to this incident.Additional evaluations were performed using the unused protector provided.Functional testing was performed for the unused sample as well.The protector was able to properly connect to a vial without issue, liquid could be withdrawn from the vial and no leakage was observed.Product undergoes visual and functional testing throughout manufacturing, including leak testing.Results were reviewed for lot 2404132 and found no problems related to the reported event.Based on the sample evaluation and quality team's investigation, we are unable to identify a root cause related to the manufacturing process at this time.It is likely the protector was not properly attached, resulting in the leak reported.The protector must be attached completely vertical to the vial during assembly.The m12 assembly fixture is recommended to ease the connection of the protector to the vial.Complaints received for this device and reported condition will continue to be tracked and trended.Our quality team regularly reviews the collected data for identification of emerging trends.
Event or Problem Description
The product leaks during use.During use.(b)(6) 2024 -bd rep - please verify where the leak occurred? between the protector and vial? between the injector and protector? is the protector assembled manually or using the assembly fixture? is this occurring with a specific medication? if yes, what medication? it leaks when you have mixed and draw up the mixture with the syringe, if you shake the mixture, it does not leak if you do not shake.They cannot be used by the machine so it has manually attached them.(b)(6) 2025: yes, customer confirmed that a mistake was made from their side and it should be sku 515102 on (b)(4).

• Brand Name: PROTECTOR P21
• Common Device Name: CLOSED ANTINEOPLASTIC AND HAZARDOUS DRUG RECONSTITUTION AND TRANSFER SYSTEM
• Manufacturer (Section D): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer (Section G): BECTON DICKINSON, S.A.; camino de valdeolivia; s/n; san agustin de guadalix
• Manufacturer Contact: helen cox (mdr) ; 75 north fairway drive; vernon hills, IL 60061 ; 8473935694
• MDR Report Key: 20924888
• Report Number: 3003152976-2024-00645
• Device Sequence Number: 5294131
• Product Code: ONB
• UDI-Device Identifier: 00382905151026
• UDI-Public: (01)00382905151026(11)240424(17)290331(10)2404132
• Combination Product (Y/N): N
• Initial Reporter Country: SW
• PMA/510(K) Number: K123213
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/28/2025

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 Catalogue Number: 515102
• Device Lot Number: 2404132
• 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: 11/29/2024
• Supplement Date Received by Manufacturer: Not provided; 03/28/2025
• Initial Report FDA Received Date: 12/13/2024
• Supplement Report FDA Received Date: 02/19/2025; 03/28/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/24/2024
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown