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All product recalls associated with Arjo, Inc..
Total Recalls
31
Past Year
0
Class I (Serious)
0
Most Recent
Feb 2023
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Repeated use of the ratchets that lock the position of the back and leg rest of the stretcher may damage the retention pin that prevents the latch from disengaging from the anchor system. This would allow the backrest to pivot freely down to the floor.
There is the potential for the slings to come apart, potentially allowing injury to the patient.
There is the potential for the slings to come apart, potentially allowing injury to the patient.
There is the potential for the slings to come apart, potentially allowing injury to the patient.
The hanger bar assembly may detach from the Maxi Move lifters with scale, due to an incorrect torque setting on the two bolts holding the scale in place.
The carabineer may not be correctly attached to the reacher and the portable patient lift may drop.
The sling ropes were manufactured with insufficient rope length past the knot to prevent the knot from coming loose.
The Kwiktrak Gate stopper may fail and allow the ceiling lift to pass through to the end of the track and fall to the floor.
The hanger bar assembly may detach from the lift during use due to fatigue failure of the bolt.
There has been an increased number of tipping incidents and subsequent patient injuries.
The hanger bar may detach from the jib yoke, and the M8 bolt in the foot pedal assembly may come loose, resulting in the patient lift becoming unstable.