MAUDE Adverse Event Report: COVIDIEN HYPO NEEDLE 25X1 1/2 A BEVEL; NEEDLE, HYPODERMIC, SINGLE LUMEN

Model Number	1188825112
Medical Device Problem Code	Fitting Problem (2183)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The complainant indicated that the device will not be returned for evaluation; therefore, a failure analysis is not available, and we are not able to determine the relationship between this device and the cause for this event.  if additional information or the sample is received, the investigation will be reopened and responded to accordingly.
Event or Problem Description
The customer reported that the needle do not thread and are often stripped.The customer further stated that, there was a connection issue with the luer of the needle.

• Brand Name: HYPO NEEDLE 25X1 1/2 A BEVEL
• Common Device Name: NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): COVIDIEN; 2010 east international speedw; deland FL 32724
• MDR Report Key: 10029170
• Report Number: 1017768-2020-00824
• Device Sequence Number: 19757196
• Product Code: FMI
• UDI-Device Identifier: 10884521007383
• UDI-Public: 10884521007383
• 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,other,use
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 05/06/2020

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: No Information
• Device Model Number: 1188825112
• Device Catalogue Number: 1188825112
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/28/2020
• Initial Report FDA Received Date: 05/06/2020
• Patient Sequence Number: 1