FDA (Devices) recall action 82607
The FDA (Devices) publishes a recall like this one as 3 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 3 pages.
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
Community Products, LLC is recalling 167 Rifton E-Pacer powered lift devices because a design change makes the load-bearing buckle springs susceptible to fatigue failure.
Community Products, LLC is recalling 3,282 Rifton TRAM Standard Base powered lift devices due to a design defect that may cause the latch mechanism to fail after repeated use.
Community Products is recalling 1,079 Rifton TRAM Low Base powered lift devices because a design change makes the latch springs susceptible to fatigue failure.