MAUDE Adverse Event Report: EMBECTA MEDICAL DEVICES (SUZHOU) CO., LTD., CHINA PN RELION 32G X 4MM 3B TW 50CT; Needle, hypodermic, single lumen

Model Number	320618
Medical Device Problem Code	Off-Label Use (1494)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This medwatch submission is both an initial and supplemental filing.Investigation of the results can be seen below: investigation summary: no samples (including photos) were returned therefore the complaint could not be confirmed and the root cause is undetermined.This is the 1st 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.Complaints received for this device and reported condition will continue to be tracked and trended.If samples are received in the future the complaint will be reopened for further investigation.Based on the above, no additional investigation and no corrective/preventative action (capa) or situational analysis (sa) is required at this time.
Event or Problem Description
Spouse of consumer reported needles bend during injection.Spouse stated that the consumer re-uses the needles, but never had an issue with other brands.Consumer refused replacement.I advised her that the needles should be used only once.Lot #: 3305033 catalog #: 320618 date of event: unknown samples: discarded.

• Brand Name: PN RELION 32G X 4MM 3B TW 50CT
• Common Device Name: Needle, hypodermic, single lumen
• Manufacturer (Section D): EMBECTA MEDICAL DEVICES (SUZHOU) CO., LTD., CHINA; CH
• Manufacturer Contact: anna garbowska-zakrzewski ; 300 kimball dr; parsippany, NJ 07054
• MDR Report Key: 22176796
• Report Number: 3027605735-2025-00036
• Device Sequence Number: 15401021
• Product Code: FMI
• UDI-Device Identifier: 00681131386791
• UDI-Public: 00681131386791
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• PMA/510(K) Number: K213478
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 06/10/2025

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: 320618
• Device Lot Number: 3305033
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/15/2025
• Initial Report FDA Received Date: 06/10/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 12/01/2023
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown