MAUDE Adverse Event Report: BECTON DICKINSON MEDICAL SYSTEMS INTERLINK LUER-LOK; NEEDLE, HYPODERMIC, SINGLE LUMEN

Catalog Number	303393
Medical Device Problem Code	Labelling, Instructions for Use or Training Problem (1318)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/27/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the bd syringe 10ml ll w/twinpak device label content was incorrect.The following information was provided by the initial reporter: material: 303393.Batch#: 5065846.Verbatim: rcc received a complaint via email.Complaint reference #: (b)(4).Correspondence language: english.Cat# of product being complained: bd303392.Description of product: syringe 5cc w/cannula st intlink 100ea/bx 4bx/ca.Lot or s/n: (b)(6) complaint category: labelling issue.Reportable: no.Incident date: (b)(6) 2025.Hospital complaint reference #: details of complaint (reported issue): "it was brought to my attention there¿s mis-label on the packaging for the 5ml syringe ref 303392.We have 7bx of 303392 (97317) 5ml but inside of the packaging is the 303393 (60902)10ml.We would like to return these; can you provide a credit for these and rga paperwork for return." please note: incident date unknown.Photos will be sent via separate email.Complaint noticed: prior to use.Problem frequency: 1st time.Customer exposure: patient injury: no.Has xxx been informed? unknown.Qty affected: (b)(4).Samples available? no.Is customer requesting an rga? no.Return qty:.
Additional Manufacturer Narrative
H.3.If a device evaluation and/or device history review is completed, a supplemental report will be filed.
Additional Manufacturer Narrative
(b)(4).Label content incorrect.No sample or photo was provided to the quality team for evaluation.However, based on previous investigations, it was confirmed that the packages contained 10ml syringes.The issue identified was a labeling discrepancy, as the top web labeling on all packages incorrectly indicated 5ml instead of 10ml.Potential root cause for the incorrect top web defect is associated with the packaging process.A corrective and preventive action (capa) will be initiated to address the issue and prevent recurrence.Furthermore, a device history record review was completed for provided lot number 5065846.A review showed no rejected inspections or quality issues during the production that could have contributed to the reported defect.Complaints received for this device and reported condition will continue to be tracked and trended.Information will be captured on trend reports and monitored monthly.Our business team regularly reviews the collected data for identification of emerging trends.
Event or Problem Description
No additional information was provided.

• Brand Name: INTERLINK LUER-LOK
• Common Device Name: NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): BECTON DICKINSON MEDICAL SYSTEMS; route 7 and grace way; canaan CT 06018
• Manufacturer (Section G): BECTON DICKINSON MEDICAL SYSTEMS; route 7 and grace way; canaan CT 06018
• Manufacturer Contact: helen cox (mdr) ; 75 north fairway drive; vernon hills, IL 60061 ; 8473935694
• MDR Report Key: 22248455
• Report Number: 1213809-2025-00415
• Device Sequence Number: 18150561
• Product Code: FMI
• UDI-Device Identifier: 00382903033935
• UDI-Public: (01)00382903033935(11)250306(17)300228(10)5065846
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K974006
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 07/30/2025

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: Other
• Device Catalogue Number: 303393
• Device Lot Number: 5065846
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/27/2025
• Supplement Date Received by Manufacturer: 07/30/2025
• Initial Report FDA Received Date: 06/17/2025
• Supplement Report FDA Received Date: 08/01/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/06/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown