MAUDE Adverse Event Report: EMBECTA MEDICAL II LLC - PARSIPPANY, NJ PEN NDL 32G 4MM PRO 90CT US; NEEDLE, HYPODERMIC, SINGLE LUMEN

Model Number	320574
Medical Device Problem Codes	Break (1069); Failure to Deliver (2338)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	12/11/2024
Type of Reportable Event	Malfunction
Event or Problem Description
Consumer reported was able to complete the flow check with this needle.However, during the injection, the needle stopped allowing the insulin to flow, clogged.Removed needle from lantus pen and could see the non-patient end needle broke off in pen.No injury to consumer.She has the needle in tape along with hub to return.(b)(6).Lot # 3017767.Catalog# 320574.Date of event december 11, 2024.Sample status awaiting sample.
Additional Manufacturer Narrative
Investigation summary: samples were received and an investigation was performed.This is the 3rd complaint for the reported lot number.A review of the manufacturing records was performed and no non-conformances were raised in association with this type of event for this lot.Embecta was able to duplicate or confirm the indicated issue as broken cannula npe.Based on trend analysis no further action is required at this time.Complaints received for this device and reported condition will continue to be tracked and trended.Based on the above, no additional investigation and corrective/preventative action (capa) or situational analysis (sa) is required.

• Brand Name: PEN NDL 32G 4MM PRO 90CT US
• Common Device Name: NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): EMBECTA MEDICAL II LLC - PARSIPPANY, NJ
• Manufacturer Contact: avital merl ; 300 kimball dr.; parsippany, NJ 07054
• MDR Report Key: 21092458
• Report Number: 3023359743-2025-00030
• Device Sequence Number: 8775709
• Product Code: FMI
• UDI-Device Identifier: 00382903205745
• UDI-Public: 00382903205745
• Combination Product (Y/N): N
• Initial Reporter State: MD
• Initial Reporter Country: US
• PMA/510(K) Number: K212015
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 03/10/2025

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: Lay User/Patient
• Device Model Number: 320574
• Device Lot Number: 3017767
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/13/2024
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/07/2025
• Supplement Report FDA Received Date: 03/10/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Female
• Patient Ethnicity: Non Hispanic
• Patient Race: White