MAUDE Adverse Event Report: BECTON DICKINSON TRAY CSE WHIT27G4.7 WE17G3.5 SWC X3795; ANESTHESIA CONDUCTION KIT

Catalog Number	405828
Medical Device Problem Code	Packaging Problem (3007)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/08/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Initial mdr submission.A follow up mdr will be submitted if additional information, a device evaluation, or a device history review is completed.
Event or Problem Description
Material #: 405828 batch#: 0001563972 it was reported by customer states that they are having issues with 2 epidural trays.In one tray, the clamps are leaking and in the other tray, the paper covering is not glued down.The customer has the tray where the paper is not glued down if needed for investigation.Ref number: 405828; lot number: 0001563972.(b)(4) is their distributor.Rcc received a complaint via phone.Pir attached customer states that they are having issues with 2 epidural trays.In one tray, the clamps are leaking and in the other tray, the paper covering is not glued down.The customer has the tray where the paper is not glued down if needed for investigation.Ref number: 405828; lot number: 0001563972.(b)(4) is their distributor.
Additional Manufacturer Narrative
(b)(4) follow up mdr for device evaluation package seal integrity: one tray was provided to our quality team for investigation.Upon initial inspection, no damage was observed with the product, the package had already been opened but the seal was observed to be complete.Functional testing was performed on the nexus connector.During our evaluations, the catheter was properly threaded into the connector without issue, proper flow was achieved, and no leakage or other issue was observed.A review of the internal manufacturing device records and raw material history files for the reported lot numbers 0001563972 was performed and no recorded quality problems or rejections related to this incident were found, all procedural and functional requirements for product release have been met.Based on the sample evaluation and quality team's investigation, a root cause cannot be established at this time.Complaints received for this device and reported condition will continue to be monitored by our quality team for signs of emerging trends.
Event or Problem Description
Material #: 405828; batch#: 0001563972.It was reported by customer states that they are having issues with 2 epidural trays.In one tray, the clamps are leaking and in the other tray, the paper covering is not glued down.The customer has the tray where the paper is not glued down if needed for investigation.Ref number: (b)(4); lot number: 0001563972.Cardinal health is their distributor verbatim: rcc received a complaint via phone.Pir attached.Customer states that they are having issues with 2 epidural trays.In one tray, the clamps are leaking and in the other tray, the paper covering is not glued down.The customer has the tray where the paper is not glued down if needed for investigation.Ref number: (b)(4); lot number: 0001563972.Cardinal health is their distributor.Epidural tray cover: july 8; i opened a case of the epidural trays and when i was removing the trays i noticed oner had the paper cover loose.There wasn't any physical damage to the box nor any unusual sound.I have the tray set aside to send back to bd._____________________________________.

• Brand Name: TRAY CSE WHIT27G4.7 WE17G3.5 SWC X3795
• Common Device Name: ANESTHESIA CONDUCTION KIT
• Manufacturer (Section D): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer (Section G): CAREFUSION, INC; 400 east foster rd; mannford OK 74044
• Manufacturer Contact: helen cox (mdr) ; 75 north fairway drive; vernon hills, IL 60061 ; 8473935694
• MDR Report Key: 19740658
• Report Number: 1625685-2024-00072
• Device Sequence Number: 3654069
• Product Code: CAZ
• UDI-Device Identifier: 00382904058289
• UDI-Public: (01)00382904058289
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: NA
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/06/2024

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 Expiration Date: 08/31/2025
• Device Catalogue Number: 405828
• Device Lot Number: 0001563972
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/08/2024
• Supplement Date Received by Manufacturer: 10/06/2024
• Initial Report FDA Received Date: 07/15/2024
• Supplement Report FDA Received Date: 10/06/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/15/2024
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown