MAUDE Adverse Event Report: BECTON DICKINSON INJECTOR LUER LOCK N35; CLOSED ANTINEOPLASTIC AND HAZARDOUS DRUG RECONSTITUTION AND TRANSFER SYSTEM

Catalog Number	515003
Medical Device Problem Code	Disconnection (1171)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/27/2024
Type of Reportable Event	Malfunction
Event or Problem Description
Material#: 515003 batch number#: unknown verbatim#: hope you had a wonderful christmas, over last 2 weeks we have 3 reported cases of leak at the connection point between icu medical tubing and phaseal injector luer lock.Hence wanted to check with you if this is something you may have heard from any other site as well.Has happened over the past few weeks--as i was made aware today.Apparently the third time was today and prompted the email to me.Based on customer response: ¿ are the pumps the icu cadd, and icu cadd sets? yes ¿ also, are the sets, fixed male luer, or a spinning collar/male swivel luer? fixed male luer ¿ the date this happened?: 12/26/24 ¿ while being used on a patient? yes ¿ what happened¿ the connection got unscrewed and extension set was disconnected ¿ what type of procedure? chemo infusion ¿ product: do you have the affected two items that leaked? were they discarded? items were discarded ¿ lot # can you please provide? and would you happen to have the packaging as well? or is the attached picture the representative lot # from the pars? attached pictures are only thing we have ¿ can you please provide the expiration date-please? not available ¿ was there any patient harm?.No immediate harm noticed, patient exposed to the 5fu he was receiving.After he manually connected the points again he went to ed to get it checked, where port was found to be functional and patient was discharged ¿ any pictures? attached earlier ¿ what is the patient outcome? patient experienced wetness, upon checking he found the dislodged connection, he thinks this lasted for about 30 minutes.He connected the points himself, went to ed to make sure and infusion was continued.The pump was unhooked after completion of infusion at infusion center later in the day.¿ are there any adverse events/serious injuries? not reported ¿ was there a delay of, or change in, the course of treatment due to the event? no ¿ what type of procedure is being performed? 5fu-pump for at home infusion.
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.The actual date of event is unknown.The date received by manufacturer was entered into the date of event field.
Additional Manufacturer Narrative
(b)(4).Follow up mdr for device evaluation: no photos or physical samples that display the reported condition were available for investigation.Product undergoes inspections throughout the manufacturing process, including testing to verify all critical dimensions are within specification.As the lot involved in this incident is unknown, a device history review could not be performed.Based on the available information we are not able to identify a root cause related to our device 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: INJECTOR LUER LOCK N35
• 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: 21103037
• Report Number: 3003152976-2025-00003
• Device Sequence Number: 15687116
• Product Code: ONB
• UDI-Device Identifier: 00382905150036
• UDI-Public: (01)00382905150036
• Combination Product (Y/N): N
• Initial Reporter State: MD
• Initial Reporter Country: US
• PMA/510(K) Number: K140591
• 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
• Report Date (Section B): 02/22/2025

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: 515003
• Device Lot Number: UNKNOWN
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/27/2024
• Supplement Date Received by Manufacturer: 02/21/2025
• Initial Report FDA Received Date: 01/08/2025
• Supplement Report FDA Received Date: 02/22/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown