MAUDE Adverse Event Report: ARJOHUNTLEIGH, INC. ROTOPRONE; BED, PATIENT ROTATION, POWERED

Model Number 209800

Device Problem No Apparent Adverse Event (3189)

Patient Problem Injury (2348)

Event Date 04/23/2020

Event Type  Injury  

Manufacturer Narrative

Please note that previous medwatch reports for this product may have been submitted under the following registration numbers: (b)(4).Currently, this product is to be handled by arjohuntleigh ab¿s complaint handling establishment and any medwatch reports will be submitted under registration (b)(4).Additional information will be provided when investigation conclusion is available.

Event Description

A patient sustained face blisters so the hospital discontinued the rotoprone therapy.No additional information had been provided.

Manufacturer Narrative

During a call concerning a patient having blisters on their cheeks (this event was submitted under mdr 9681684-2020-00029), the nurse stated that earlier they had another patient with face blisters, and thus decided to discontinue the rotoprone therapy.This report concerns allegation made by the nurse about the earliest patient.The rotoprone bed returned to service center the same day and two days later was rented for another facility.There was no repairs completed on the bed between the rental period.Due to covid -19 no more information, regarding seriousness of these injuries, was made available.Product instruction for use 208662-ah rev e states: - ¿skin care - fitting the head support, face pack, proning packs or other accessory packs too tightly may increase pressure points, possibly leading to skin breakdown.Assess skin at frequent intervals depending on patient condition (at least once every four hours).Give extra attention to skin at pressure points and locations where moisture or incontinence may occur or collect.Common pressure points include, but are not limited to, the face, ears, axilla, shoulders, sides and upper and lower extremities.Early intervention may be essential to preventing serious skin breakdown.Do not leave patient in a stationary position in the supine or prone position for more than two hours.¿ - ¿face pack ¿ position face pack to ensure visibility of the eyes and to avoid pressure on or around patient¿s eyes, mouth and ears.Remove face pack at regular intervals to assess the eyes, ears and facial skin.Prolonged, increased intraocular pressure may cause eye injury, including blindness.Ensure all face pack buckles are secure before proning patient¿.- ¿face pack should be positioned as low on the patient¿s brow as possible without causing pressure on or around the patient¿s eyes, nose or mouth¿.Ifu includes also guidelines and steps that can be considered when managing potential skin complications that can be associated with prone therapy.The rotoprone therapy system is a patient care system for the prevention and treatment of complications associated with immobility.Although the use of the device is designed to help caregivers address potentially life-threatening conditions, proning itself may present inherent risk of injury.Caregivers should always address and discuss safety information, risks and precautions with the patient (or the patient¿s legal guardians) and the patient¿s family.The device was used for patient treatment when the event occurred, therefore played a role in the event, but there was no device failure.We report it in abundance of caution because of limited information received.

• Brand Name: ROTOPRONE
• Type of Device: BED, PATIENT ROTATION, POWERED
• Manufacturer (Section D): ARJOHUNTLEIGH, INC.; 4958 stout drive; san antonio TX 78219
• MDR Report Key: 10082680
• MDR Text Key: 192156955
• Report Number: 9681684-2020-00030
• Device Sequence Number: 1
• Product Code: IKZ
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,user f
• Type of Report: Initial,Followup
• Report Date: 06/19/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/22/2020
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 209800
• Was Device Available for Evaluation?: Yes
• Date Manufacturer Received: 05/21/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other