MAUDE Adverse Event Report: Parker Medical Parker; Endotracheal Tube, High Volume Low Pressure (PFHV), Cuffed, Parker, 8.0mm

Model Number	H-PFHV-80 (I-PFHV-80)
Medical Device Problem Code	Gas/Air Leak (2946)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/18/2026
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the inflation port of the endotracheal tube (ett) did not seem to be holding pressure, and they elected to extubate the patient.Multiple attempts were made to reintubate the patient using orogastric tube (ogt)/nasogastric tube (ngt) without success; the patient reportedly had a lot of secretions and blood in the oropharynx.Once the patient was successfully reintubated the ventilator alarm stopped and the carbon dioxide (co2) trace was fine.No additional information, concerning patient outcome, was provided.
Additional Manufacturer Narrative
The product involved in the report has not been returned.A review of the device history record is in-progress.All information reasonably known as of 29 july 2026 has been included in the health authority report.Should additional information be obtained a follow-up health authority report will be provided.The information provided by airlife.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 airlife.Airlife 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 airlife complaint database and is identified as complaint (b)(4).This information is submitted pursuant to 21cfr803, in compliance with the medical device reporting requirement and should not be considered to be an admission that a airlife product is defective or causes serious injury risk assessment the ultimate risk is low, as that is the highest risk of the patient/caregiver and regulatory/compliance considerations: (1) patient/ caregiver performed risk assessment with rma-20024b, rev 3; the complaint most closely aligns with risk id r25 with a potential cause of hazard being " 1.Check valve leak 2.Cuff having pin hole 3.Damaged tubing 4.Leaky bonds".Severity = 6, likelihood of occurrence = 2, calculated occurrence = 0.0012% per ref-20001-c1 rev 2, these levels indicate low risk.(2) regulatory/ compliance reviewed ref-20001-c1 rev 2, and there is low regulatory/ compliance risk.(3) brand recognition and customer impact reviewed ref-20001-c1 rev 2, and there is low brand recognition/customer impact.Device history record (dhr) review based on the device history record (dhr) review there were no abnormal processing issues noted.All products/packaging were produced per the approved manufacturing procedures, specifications, and inspections.Complaint history review the complaint history was reviewed in grand avenue from reported dates 06/29/2024 through 06/29/2026, for part number i-pfhv-80 and failure mode a050402 - gas/air leak.There were 1 other complaints reported for the same issue and part number under during the same timeframe; (b)(4).Sales = (b)(4) ea calculated occurrence (p1) =(2 complaint(s) / (b)(4) ea sold) x 100 = 0.0012% occurrence ranking = low (3).

• Brand Name: Parker
• Common Device Name: Endotracheal Tube, High Volume Low Pressure (PFHV), Cuffed, Parker, 8.0mm
• Manufacturer (Section D): Parker Medical; 9457 s university blvd; pmb 331; highlands ranch CO 80126
• Manufacturer (Section G): Well Lead Medical Co; c-4 jinhu industrial estate; hualong; panyu, guangzhou 51143 4; JA 511434
• Manufacturer Contact: melissa brickley ; 2710 northridge dr nw suite a; grand rapids, MI 49544 ; +1(616)259-8415
• MDR Report Key: 50078240
• Report Number: 3004748541-2026-00140
• Device Sequence Number: 10753684
• Product Code: BTR
• UDI-Device Identifier: 00607411952753
• UDI-Public: (01)00607411952753(10)2601HV0075M
• Combination Product (Y/N): N
• Initial Reporter Country: NZ
• PMA/510(K) Number: K984528
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative,Distributor
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 09/24/2026

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 Model Number: H-PFHV-80 (I-PFHV-80)
• Device Catalogue Number: H-PFHV-80 (I-PFHV-80)
• Device Lot Number: 2601HV0075M
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/29/2026
• Supplement Date Received by Manufacturer: 06/29/2026; 09/23/2026
• Initial Report FDA Received Date: 07/30/2026
• Supplement Report FDA Received Date: 09/17/2026; 09/25/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown