MAUDE Adverse Event Report: BECTON DICKINSON, S.A. PHASEAL OPTIMA; CLOSED ANTINEOPLASTIC AND HAZARDOUS DRUG RECONSTITUTION AND TRANSFER SYSTEM

Catalog Number	515070
Medical Device Problem Code	Leak/Splash (1354)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/20/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the bd connector c35-o had leakage at the luer.The following information was provided by the initial reporter: material#: 515056, 515070, batch#: unknown.Complaint via email.We are experiencing issues with the bd phaseal optima injector n40 0 and the bd phaseal optima infusion connector c35 0 leaking at the connection site with iv tubing.(b d515056 and b d515070) is this a previously reported issue? is this a known issue with a solution? should we sequester and send back the affected lots?.
Additional Manufacturer Narrative
B.3.The date received by manufacturer has been used for this field.H.3.If a device evaluation and/or device history review is completed, a supplemental report will be filed.
Additional Manufacturer Narrative
(b)(4) follow up mdr for device evaluation: it was reported that leakage occurred at the tubing connection site involving the c35-o optima connector and the n40-o optima locking injector.Five photographs were provided to the quality team for investigation.Review of the photographs showed that both the c35-o and n40-o were assembled to a mating device, and no issues with the connection could be identified.Gauze was observed wrapped around the connection between the n40-o and the mating tubing, with a white residue observed near the connection area, suggesting a leak may have occurred.There is no visible damage or other defect identified to indicate why there may have been a leakage.A device history record review was conducted for injector lot 2503736 and connector lot 2506503.No deviations or nonconformances were identified during the manufacturing process that could have contributed to the reported concern.Products undergo multiple inspections throughout the manufacturing process to ensure quality and functionality, including verification of all critical dimensions such as luer threading.Results for the reported lots were reviewed, and no issues related to the event were found.Retained samples of each lot were also used for evaluation.All product was inspected, no damage or defects were observed on the luer threading and dimensional testing verified the product met required specification.Based on our investigation along with the photo evaluation, review of device records, and analysis of the retained samples we were unable to identify a root cause related to the product or manufacturing process at this time.Complaints received for this device and reported condition will be monitored by our quality team for signs of emerging trends.
Event or Problem Description
No additional information.

• Brand Name: PHASEAL OPTIMA
• Common Device Name: CLOSED ANTINEOPLASTIC AND HAZARDOUS DRUG RECONSTITUTION AND TRANSFER SYSTEM
• Manufacturer (Section D): BECTON DICKINSON, S.A.; camino de valdeolivia; s/n; san agustin de guadalix
• 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: 24783841
• Report Number: 3003152976-2026-00171
• Device Sequence Number: 6133544
• Product Code: ONB
• UDI-Device Identifier: 00382905150708
• UDI-Public: (01)00382905150708(11)250626(17)270531(10)2506503
• Combination Product (Y/N): N
• Initial Reporter State: OR
• Initial Reporter Country: US
• PMA/510(K) Number: K181221
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 04/20/2026

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: 515070
• Device Lot Number: 2506503
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/25/2026
• Supplement Date Received by Manufacturer: Not provided; 04/20/2026
• Initial Report FDA Received Date: 04/03/2026
• Supplement Report FDA Received Date: 04/07/2026; 04/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/26/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown