Maxi Move Scoop Stretcher; Note: The stretcher is an accessory to the Maxi Move Patient Lift; Made by Arjo Hospital Equi

FDA device recall Z-2230-2009 · posted 2009-09-22 · Terminated

Recall details

Recalling firm

ArjoHuntleigh

Reason for recall

A Scoop Stretcher is made up of two frames that are held together with two locking devices, one on each end. Each locking device contains a safety latch. The safety latch could unintentionally release when the side frames are pulled for positioning.

Action taken

ArjoHuntleigh sent their customers a cover letter and the Field Safety Notification, informing them of the potential problem with the safety latches on the stretcher and a pending visit from an ArjoHuntleigh Service Technician to correct the problem. These letters were sent via UPS 2nd day delivery on 8/18/09. The customers were requested to test their stretchers upon receipt of the letter following the instructions for checking the safety latches on the stretcher: * Place the stretcher on its side on a non-scratch surface. * Try to pull the two sides apart with the safety latch engaged. * Test both the head and foot ends of the stretcher. * If the stretcher pulls apart, remove it from use immediately. It is important to note that all affected stretchers will be upgraded, whether they fail the test or not.

Root cause

Manufacturing material removal

Status

Terminated

Product code

FSA

Quantity affected

214 units

Distribution

Worldwide Distribution

Date initiated

2009-08-18

Date posted

2009-09-22

Date terminated

2010-01-07

Location

Addison, IL