MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP - EXCELSIOR; DBD-SYRINGE, 2.5ML SALINE IN 3ML

Catalog Number	EMZE010030
Medical Device Problem Code	Short Fill (1575)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/18/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
It was reported that the syringe was filled to "1 ml instead of 2.5 ml".The customer did not report any patient involvement, cancelation/delay of procedure, or adverse event related to the reported incident.No additional details are available related to the customer reported issue.To date, no information has been received to indicate that a user or a patient experienced a death, serious injury, medical intervention, follow-up care, or other adverse health impact associated with the reported problem/issue.In an abundance of caution, and in response to an fda 483 issued for cfn 1417592 on 22-jan-2024, this medwatch is being filed for the reported problem/issue.If additional relevant information becomes available a supplemental medwatch will be filed.
Event or Problem Description
It was reported that the syringe was filled to "1 ml instead of 2.5 ml".
Additional Manufacturer Narrative
Update to h6: investigation findings.Update to h6: investigation conclusions.

• Common Device Name: DBD-SYRINGE, 2.5ML SALINE IN 3ML
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP - EXCELSIOR; 1933 heck avenue; neptune NJ 07753 4428
• Manufacturer Contact: danielle tognocchi ; three lakes drive; northfield, IL 60093
• MDR Report Key: 22835768
• Report Number: 2027791-2025-00015
• Device Sequence Number: 9934237
• Product Code: NGT
• UDI-Device Identifier: 00363807100305
• UDI-Public: 00363807100305
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 11/13/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: EMZE010030
• Device Lot Number: 3145506
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/31/2025
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/21/2025
• Supplement Date Received by Manufacturer: 11/04/2025
• Initial Report FDA Received Date: 08/18/2025
• Supplement Report FDA Received Date: 11/13/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/07/2025
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown