MAUDE Adverse Event Report: VENTEC LIFE SYSTEMS, INC VOCSN PATIENT BREATHING PACKAGE; VENTILATOR, CONTINUOUS, FACILITY USE

Model Number	PEDIATRIC, ACTIVE, OXYGEN, BLUE
Medical Device Problem Code	Material Integrity Problem (2978)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/21/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported to ventec that the clear film wall of a breathing circuit had detached from the blue polypropylene spiral portion of the patient circuit (pediatric, active, oxygen, blue) assembly.The reported issue was discovered during incoming inspection.There were no reports of patient involvement associated with the reported event.Section d4 model number, catalog number and lot code reflects the information known about the patient circuit.The udi was unavailable at the time of this submission, therefore section d4 udi is "unknown", and section h4 date of manufacturer will be left blank.
Additional Manufacturer Narrative
H6: ventec continues to investigate the reported issue.A follow-up report will be submitted when the investigation is complete as defined by 21 cfr 803.56.
Additional Manufacturer Narrative
Corrected information for supplemental medwatch report 001 ¿ section d4, model # and catalog # of the initial medwatch report stated: prt-00802-000 section d4, model # and catalog # of the initial medwatch report should have stated: prt-00802-001.New information for supplemental medwatch report 001 ¿ h6: udi information for the patient circuit was confirmed.Section d4, unique identifier (udi) #, and section h4, date of manufacturer, have been updated accordingly.The patient circuit was returned to ventec.Ventec evaluated the patient circuit and observed that the inner clear tubing was delaminating (detaching) from the blue spiral reinforcement.The degree of delamination appeared to vary throughout the length of the circuit based on visual observation and tactile handling of the bond.Ventec contacted the contract manufacturer of the product (supplier) regarding the reported issue.The supplier later advised ventec that it had performed an internal investigation and determined that the product was manufactured using inadequate extrusion temperature.Please reference ventec corrections and removals report number (b)(4).Ventec was unable to enter and transmit the corrections and removals number in section h9 due to system character limits in that field.
Additional Manufacturer Narrative
Section d1, brand name, of the initial medwatch report stated: vocsn.Section d1, brand name, of the initial medwatch report should have stated: vocsn patient breathing package.Section d4, model #, of supplemental medwatch report 001 stated: prt-00802-001.Section d4, model #, of supplemental medwatch report 001 should have stated: pediatric, active, oxygen, blue.Section d4, udi #, of supplemental medwatch report 001 stated: (b)(4).Section d4, udi #, of supplemental medwatch report 001 should have stated: (b)(4).Section h5, labeled for single use, of the initial medwatch report stated: no.Section h5, labeled for single use, of the initial medwatch report should have stated: yes.

• Brand Name: VOCSN PATIENT BREATHING PACKAGE
• Common Device Name: VENTILATOR, CONTINUOUS, FACILITY USE
• Manufacturer (Section D): VENTEC LIFE SYSTEMS, INC; 22002 26th ave se; bothell WA 98021
• Manufacturer (Section G): VENTEC LIFE SYSTEMS, INC; 22002 26th ave se; bothell WA 98021
• Manufacturer Contact: elizabeth gilbert ; 22002 26th ave se; bothell, WA 98021 ; 4256861765
• MDR Report Key: 18288775
• Report Number: 3013095415-2023-00807
• Device Sequence Number: 6696356
• Product Code: CBK
• UDI-Device Identifier: 00855573007587
• UDI-Public: (01)00855573007587(11)220307(10)220922
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K162877
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Remedial Action: Recall
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 11/10/2023

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
• Device Model Number: PEDIATRIC, ACTIVE, OXYGEN, BLUE
• Device Catalogue Number: PRT-00802-001
• Device Lot Number: 220922
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/04/2023
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/10/2023
• Supplement Date Received by Manufacturer: 12/08/2023; 07/17/2024
• Initial Report FDA Received Date: 12/07/2023
• Supplement Report FDA Received Date: 01/04/2024; 07/19/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 03/07/2022
• 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: Unknown
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: SEE H10
• Patient Sequence Number: 1
• Patient Sex: Unknown