MAUDE Adverse Event Report: MYCO MEDICAL SUPPLIES, INC MCKESSON BRANDS; NEEDLE, SPINAL QUINCKE 22GX5"

Catalog Number	4633V2
Medical Device Problem Code	Complete Blockage (1094)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/12/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported by the customer that they were experiencing an issue during an injection; the spinal needle would not allow the medication to deploy, even after attempting to reinsert the stylet into the needle.No information was received regarding a serious injury as a result of this product issue.

• Brand Name: MCKESSON BRANDS
• Common Device Name: NEEDLE, SPINAL QUINCKE 22GX5"
• Manufacturer (Section D): MYCO MEDICAL SUPPLIES, INC; 158 toverview court; cary NC 27513
• MDR Report Key: 21512393
• Report Number: 1451040-2025-00007
• Device Sequence Number: 4400680
• Product Code: BSP
• UDI-Device Identifier: 10612479201597
• UDI-Public: 10612479201597
• Combination Product (Y/N): N
• Initial Reporter State: NE
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/04/2025
• Report Date (Section F): 03/04/2025

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: Health Professional
• Device Catalogue Number: 4633V2
• Device Lot Number: 2208889
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 02/12/2025
• Device Age: 12 MO
• Event Location: Outpatient Treatment Facility
• Date Report to Manufacturer: 03/04/2025
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 03/04/2025
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown
• Date Report Sent to FDA: 03/04/2025