MAUDE Adverse Event Report: COOK INC DIECKMANN INTRAOSSEOUS INFUSION NEEDLE; FMI NEEDLE, HYPODERMIC, SINGLE LUMEN

Catalog Number	C-DIN-16-2.5-T45-DKM
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	04/14/2015
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
Event or Problem Description
It was reported that when the physician punctured for the bone marrow with intraosseous needle urgently, it bent and could not be used for transfusion.The complaint device was replaced with another device.It was further noted that the cannula had been dislodged from its glue joint with the winged hub.No other information was made available.

• Brand Name: DIECKMANN INTRAOSSEOUS INFUSION NEEDLE
• Common Device Name: FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• MDR Report Key: 8170849
• Report Number: 1820334-2018-03826
• Device Sequence Number: 11183567
• Product Code: FMI
• UDI-Device Identifier: 00827002059863
• UDI-Public: (01)00827002059863(17)171201(10)3973966
• Combination Product (Y/N): N
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,o
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 12/17/2018

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 Expiration Date: 12/01/2017
• Device Catalogue Number: C-DIN-16-2.5-T45-DKM
• Device Lot Number: 3973966
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/05/2015
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/14/2018
• Initial Report FDA Received Date: 12/17/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1