MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP; KIT,HUMID,AQUAPAK,540ML,H2O, ADPT

Catalog Number	HUD00540
Medical Device Problem Code	Connection Problem (2900)
Health Effect - Clinical Code	Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Date of Event	06/08/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
According to the facility on 06/08/2024 "patient's trach noted to be plugged requiring additional interventions to resolve".Per the facility the registered nurse "found humidification bottle to not be working correctly which resulted in drying out the patient's airway".Per the facility the registered nurse "observed no humidification coming out despite bottle being spiked and fluid in bottle bubbling".No additional information is available at this time.It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.
Event or Problem Description
According to the facility on 06/08/2024 "patient's trach noted to be plugged requiring additional interventions to resolve".

• Common Device Name: KIT,HUMID,AQUAPAK,540ML,H2O, ADPT
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093
• Manufacturer Contact: justin herrmann ; three lakes drive; northfield, IL 60093
• MDR Report Key: 20728825
• Report Number: 1417592-2024-00966
• Device Sequence Number: 8941326
• Product Code: BTT
• UDI-Device Identifier: 20197344007155
• UDI-Public: 20197344007155
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 11/19/2024

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?: No
• Device Catalogue Number: HUD00540
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/01/2024
• Initial Report FDA Received Date: 11/19/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown