MAUDE Adverse Event Report: CARDINAL HEALTH NEEDLE SAFETY HYPODERMIC MAGELLAN STERIL; NEEDLE, HYPODERMIC, SINGLE LUMEN

Model Number	8881850515
Medical Device Problem Codes	Use of Device Problem (1670); Fail-Safe Did Not Operate (4046)
Health Effect - Clinical Codes	Exposure to Body Fluids (1745); Needle Stick/Puncture (2462)
Date of Event	05/24/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
An investigation is currently underway.Upon completion, the results will be forwarded.
Event or Problem Description
Customer reports: our staff has encountered issues with the magellan 25g needle.Our nurse had a needle stick after injecting meds to a hiv positive patient.She followed the correct safety technique.However, the needle bent out while she was pressing the safety glide.The needle is too flimsy so that it cannot support the glide.The incident was entered in the cedars sinai safe for further investigation and for tracking purposes if it warrants pulling it from our supplies.
Additional Manufacturer Narrative
Based on the information available to us, we were unable to confirm the event.In the meantime, all information received will be used for further tracking and trending purposes.

• Brand Name: NEEDLE SAFETY HYPODERMIC MAGELLAN STERIL
• Common Device Name: NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): CARDINAL HEALTH; 777 west street; mansfield MA 02048
• Manufacturer (Section G): CARDINAL HEALTH; 2010 east international speedw; deland FL 32724
• Manufacturer Contact: jill saraiva ; 777 west street; mansfield, MA 02048 ; 5086183640
• MDR Report Key: 17159758
• Report Number: 1017768-2023-01065
• Device Sequence Number: 12216906
• Product Code: FMI
• UDI-Device Identifier: 10884521145047
• UDI-Public: 10884521145047
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/24/2023

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
• Device Model Number: 8881850515
• Device Catalogue Number: 8881850515
• Device Lot Number: 23A311
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/25/2023
• Supplement Date Received by Manufacturer: 05/25/2023
• Initial Report FDA Received Date: 06/19/2023
• Supplement Report FDA Received Date: 10/24/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown