MAUDE Adverse Event Report: AMBU A/S AMBU SPUR II PEDIATRIC RESUSCITATOR; MANUAL RESUSCITATOR

Model Number	531600051
Medical Device Problem Code	Blocked Connection (2888)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/28/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The reported failure is verified based on the 2 returned samples.The defect was caused due to a damaged tool pin during the molding process for the patient valve housing.The blocked manometer port was not detected by the function tests performed in the spur ii assembly line.To mitigate that this defect occurs again a corrective action (ca-000948) has been initiated.The molding tool has been repaired and a quality control check point on the manometer port has now been added into the working instructions for the injection control procedure for the patient valve housing.In addition, requirements to verify that the test equipment used to test 'manometer port passage' is efficient, has been added.Ambu will keep monitoring the issue and take actions as appropriate.
Event or Problem Description
Customer was checking the inventory before the spur ii product went into circulation.A defect in several ambu pediatric resuscitation bags, specifically in the pressure manometer port, was detected.The manometer port being obstructed, rendered the manometer nonfunctional.

• Brand Name: AMBU SPUR II PEDIATRIC RESUSCITATOR
• Common Device Name: MANUAL RESUSCITATOR
• Manufacturer (Section D): AMBU A/S; baltorpbakken 13; ballerup, dnk 2750 ; DA 2750
• MDR Report Key: 22135566
• Report Number: 1220828-2025-00012
• Device Sequence Number: 7357415
• Product Code: OEV
• UDI-Device Identifier: 05707480163441
• UDI-Public: 05707480163441
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 06/03/2025
• Report Date (Section F): 06/03/2025

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: 531600051
• Device Catalogue Number: 531600051
• Device Lot Number: 2000015181
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/19/2025
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 04/28/2025
• Event Location: Hospital
• Date Report to Manufacturer: 06/03/2025
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 06/03/2025
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown