MAUDE Adverse Event Report: BD MEDICAL (BD WEST) MEDICAL SURGICAL BD PRECISIONGLIDE¿ 27 G X 1-1/4" HYPODERMIC NEEDLES; HYPODERMIC SINGLE LUMEN NEEDLE

Model Number	305136
Medical Device Problem Code	Complete Blockage (1094)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/02/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported while using bd precisionglide¿ 27 g x 1-1/4" hypodermic needles the needle was clogged.There was no report of patient impact.The following information was provided by the initial reporter: material#: 305136, batch#: 2175216.It was reported by customer that 27 g 1.5¿ needles (clogged ¿ would not infuse) x 2 separate kits.Complaint number - (b)(4).Created date - 03-03-23.Event date - (b)(6) 2023.Manufacturing site - jrz.Product malfunction/failure mode - defective component.Product description summary - 27 g 1.5¿ needles (clogged ¿ would not infuse) x 2 separate kits.Complaint quantity - 2.Mfg.Sku number - 305136.Component name - disc sug bf301629 (021723)ndl,27gx1-1/4in,precisionglide.Investigated component lot number - 2175216.Was there an injury - no.Was there a death - no.
Additional Manufacturer Narrative
Investigation summary: a device history record review was completed by our quality engineer team for provided material number 305136 and lot number 2175216.The review did not reveal any detected abnormalities during the production process that could have contributed to this defect and all quality tests were found to be within specification.As a sample was unavailable for return, a thorough sample investigation could not be completed.Based on the investigation results, an exact cause for this incident could not be identified.

• Brand Name: BD PRECISIONGLIDE¿ 27 G X 1-1/4" HYPODERMIC NEEDLES
• Common Device Name: HYPODERMIC SINGLE LUMEN NEEDLE
• Manufacturer (Section D): BD MEDICAL (BD WEST) MEDICAL SURGICAL; 1852 10th avenue; columbus NE 68601
• Manufacturer (Section G): BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.; 9450 south state street; sandy UT 84070
• Manufacturer Contact: phillip emmert ; 1852 10th avenue; columbus, NE 68601 ; 8015652341
• MDR Report Key: 16635757
• Report Number: 1911916-2023-00186
• Device Sequence Number: 7150132
• Product Code: FMI
• UDI-Device Identifier: 30382903051367
• UDI-Public: (01)30382903051367
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: K021475
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/13/2023

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
• Operator of Device: Other
• Device Model Number: 305136
• Device Catalogue Number: 305136
• Device Lot Number: 2175216
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/07/2023
• Initial Report FDA Received Date: 03/29/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 06/24/2022
• 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