MAUDE Adverse Event Report: ARJOHUNTLEIGH, INC. MAXXAIR ETS; MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE

Model Number 47129

Device Problem Deflation Problem (1149)

Patient Problem Pressure Sores (2326)

Event Date 12/18/2023

Event Type  Injury  

Manufacturer Narrative

The investigation is in progress.The conclusions will be provided within the manufacturer's follow-up report.Once the investigation is completed.

Event Description

Arjo became aware of the event involving the maxxair ets mattress installed on citadel plus bed frame.The customer reported that the mattress was dipping and not inflating properly.The patient developed stage 4 pressure injury to right buttock.The mattress was swapped out and inspected.No faults were found.

• Brand Name: MAXXAIR ETS
• Type of Device: MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE
• Manufacturer (Section D): ARJOHUNTLEIGH, INC.; 4958 stout drive; san antonio TX 78219
• MDR Report Key: 18666679
• MDR Text Key: 334837762
• Report Number: 1419652-2024-00018
• Device Sequence Number: 1
• Product Code: FNM
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Distributor
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 02/08/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/08/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 47129
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 02/08/2024
• Distributor Facility Aware Date: 01/10/2024
• Date Report to Manufacturer: 02/08/2024
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Hospitalization
• Patient Age: 65 YR
• Patient Sex: Male
• Patient Weight: 109 KG