MAUDE Adverse Event Report: ALLIED HEALTHCARE PRODUCT INC. ALLIED; AHP300

Model Number	AHP300
Medical Device Problem Code	Inaccurate Delivery (2339)
Health Effect - Clinical Code	Hypoventilation (1916)
Date of Event	10/19/2022
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The unit was returned for repair and was recalibrated and tested.It met all specifications after the calibration was completed.
Event or Problem Description
From the paramedic who witnessed the malfunction: the ventilator had strange issue of the pip suddenly showing 6 wothout changing from that number a worsening in patient condition.I had to tap the screen which made it start to work again.It happened again on the transport and again tapping it worked.The vent was pulled offline.

• Brand Name: ALLIED
• Common Device Name: AHP300
• Manufacturer (Section D): ALLIED HEALTHCARE PRODUCT INC.; 1720 sublette ave; st. louis MO 63110
• Manufacturer (Section G): ALLIED HEALTHCARE PRODUCT INC.; 1720 sublette ave; st. louis MO 63110
• Manufacturer Contact: nicole szakats ; 1720 sublette ave; st. louis, MO 63110 ; 3147712400
• MDR Report Key: 20274042
• Report Number: 1924066-2024-00082
• Device Sequence Number: 12591378
• Product Code: BTL
• UDI-Device Identifier: 00026072000014
• UDI-Public: (01)00026072000014
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: K132021
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Administrator/Supervisor
• Remedial Action: Repair
• Type of Report: Initial
• Report Date (Section B): 09/12/2024

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
• Device Model Number: AHP300
• Device Catalogue Number: AHP300
• Device Lot Number: NO
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 10/19/2022
• Initial Report FDA Received Date: 09/20/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 01/11/2019
• Is the Device Labeled for Single Use? (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
• Patient Sex: Unknown