MAUDE Adverse Event Report: CAREFUSION, INC BD TRAY EPID CONT WE18G3.5 C20 LOR5 S/L/L-E; ANESTHESIA CONDUCTION KIT

Catalog Number	406047
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	08/18/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Initial reporter phone #: unknown.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
Event or Problem Description
It was reported that the catheter cannot thread through the needle with a bd tray epid cont we18g3.5 c20 lor5 s/l/l-e.The following information was provided by the company reporter: it was reported that customer is not able to pass catheter through needle.The following information was provided by the initial reporter: most of my complaints were minor in nature and have been ongoing for a number of months now but in the recent past i have noticed increasing resistance to passage of the catheter thru the needle.It is now to a point where i cannot pass it at all.I check each time before i place a needle into a patient now and have had several kits where you cannot pass the catheter, one of which you cannot even get one centimeter past the hub.
Additional Manufacturer Narrative
Investigation summary: a review of the device history records identified no issues for lot 0001285103.Sample analysis confirmed the failure mode (incorrect component).The sample returned contained the incorrect 19 gauge epidural catheter.The investigation noted that packaging of the 406047 is a manual process.As part of this manufacturing process, all components are to be verified with the applicable bill of material at start up and at any time during the manufacturing process when more components are delivered to the manufacturing line.Based on the dhr review results and the sample evaluation, the investigation identified the most probable root cause to be a failure in the component verification step with the applicable bill of materials during the manufacture of the affected finished good lot.Conclusion: based on the complaint investigation, the most probable root cause was that manufacturing personnel did not properly verify components as they were delivered to the manufacturing line.Based on the identified probable root cause, all applicable manufacturing associates have received awareness training regarding this particular incident.Awareness training for this issue was done previously for this lot and failure mode.
Event or Problem Description
It was reported that the catheter cannot thread through the needle with a bd tray epid cont we18g3.5 c20 lor5 s/l/l-e.The following information was provided by the company reporter: it was reported that customer is not able to pass catheter through needle.The following information was provided by the initial reporter: most of my complaints were minor in nature and have been ongoing for a number of months now but in the recent past i have noticed increasing resistance to passage of the catheter thru the needle.It is now to a point where i cannot pass it at all.I check each time before i place a needle into a patient now and have had several kits where you cannot pass the catheter, one of which you cannot even get one centimeter past the hub.

• Brand Name: BD TRAY EPID CONT WE18G3.5 C20 LOR5 S/L/L-E
• Common Device Name: ANESTHESIA CONDUCTION KIT
• Manufacturer (Section D): CAREFUSION, INC; 400 east foster rd; mannford OK 74044
• MDR Report Key: 8965405
• Report Number: 1625685-2019-00101
• Device Sequence Number: 2521339
• Product Code: CAZ
• UDI-Device Identifier: 00382904060473
• UDI-Public: 00382904060473
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: DISCRETION
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,other,use
• Initial Reporter Occupation: Nurse
• Type of Report: Initial,Followup
• Report Date (Section B): 09/18/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Expiration Date: 09/30/2020
• Device Catalogue Number: 406047
• Device Lot Number: 0001285103
• Initial Date Received by Manufacturer: 08/19/2019
• Supplement Date Received by Manufacturer: 08/19/2019
• Initial Report FDA Received Date: 09/05/2019
• Supplement Report FDA Received Date: 09/18/2019
• 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