MAUDE Adverse Event Report: HALYARD HEALTH KIMVENT 24-HOUR ORAL CARE KIT Q2 WITH CHG; VAP ORAL CARE PRODUCTS

Model Number	97012
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	03/30/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The actual complaint product was not returned for evaluation.A review of the device history record is not possible as no lot number was provided.Root cause could not be determined.All information reasonably known as of (b)(6) 2017 has been included in this health authority report.Should additional information be obtained, a follow-up health authority report will be provided.The information provided by halyard health represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to halyard health.Halyard health has no independent knowledge of the event reported but is relaying the information that was provided by the user facility where the incident occurred.This product incident is documented in the halyard health complaint database and identified as complaint comp-(b)(4).
Event or Problem Description
It was reported while performing oral care on a patient who mouth was dry and sticky the suction swab broke off on the curved area and into the patient¿s mouth.The speech pathologist was able to remove the swab from the patient¿s mouth.Additional information was received on (b)(6) 2017 stated the swab broke with the entire stem falling into the patient¿s oral cavity.No additional information was provided.

• Brand Name: KIMVENT 24-HOUR ORAL CARE KIT Q2 WITH CHG
• Common Device Name: VAP ORAL CARE PRODUCTS
• Manufacturer (Section D): HALYARD HEALTH; 5405 windward parkway; alpharetta GA 30004
• MDR Report Key: 6482352
• Report Number: 3006646024-2017-00010
• Device Sequence Number: 16365051
• Product Code: EFW
• UDI-Device Identifier: 30680651139048
• UDI-Public: 30680651139048
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/30/2017

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 Health Care Professional
• Device Model Number: 97012
• Device Catalogue Number: 991013904
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/30/2017
• Initial Report FDA Received Date: 04/11/2017
• Patient Sequence Number: 1
• Patient Age: 86 YR
• Patient Weight: 63