MAUDE Adverse Event Report: ICU Medical Healthcare Manufacturing S.A. de C.V. Jelco Hypodermic Needle-Pro w/Syringe; Needle, hypodermic, single lumen

Catalog Number	EL31915
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/11/2026
Type of Reportable Event	Malfunction

• Brand Name: Jelco Hypodermic Needle-Pro w/Syringe
• Common Device Name: Needle, hypodermic, single lumen
• Manufacturer (Section D): ICU Medical Healthcare Manufacturing S.A. de C.V.; carretera miguel alemán km21.7; parque industrial monterrey; apodaca nuevo leon NA 66603 ; MX 66603
• Manufacturer Contact: reed covert ; carretera miguel alemán km21.7; parque industrial monterrey; apodaca nuevo leon, NA 66603 ; MX 66603 ; +1(224)706-2300
• MDR Report Key: 50573028
• Report Number: 9616567-2026-00017
• Device Sequence Number: 10293916
• Product Code: FMI
• UDI-Device Identifier: 00351688072545
• Combination Product (Y/N): N
• Initial Reporter State: NA
• Initial Reporter Country: GM
• PMA/510(K) Number: K923127
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 09/02/2026

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: EL31915
• Device Lot Number: 6064774
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/15/2026
• Initial Report FDA Received Date: 09/02/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown