MAUDE Adverse Event Report: BECTON, DICKINSON, AND COMPANY BD PRECISIONGLIDE NEEDLE 25G X 1 1/2"; NEEDLE, HYPODERMIC, SINGLE LUMEN

Catalog Number	305127
Health Effect - Clinical Code	Needle Stick/Puncture (2462)
Date of Event	03/25/2024
Type of Reportable Event	Malfunction
Event or Problem Description
During a surgical case, the perioperative nurse was stuck with a bd 25gx1.5 needle due to a malfunction of the needle.A picture is attached of the needle.Reference report #mw5153344.

• Brand Name: BD PRECISIONGLIDE NEEDLE 25G X 1 1/2"
• Common Device Name: NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): BECTON, DICKINSON, AND COMPANY
• MDR Report Key: 19002612
• Report Number: MW5153343
• Device Sequence Number: 3880081
• Product Code: FMI
• UDI-Device Identifier: 00382903051274
• UDI-Public: 00382903051274
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Voluntary
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/26/2024

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: 305127
• Device Lot Number: 3237171
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 03/28/2024
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown