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Med-Mizer, Inc. recalls Med-Riser MR600 Patient Lift
Recalled March 8, 2023 · FDA recall Z-1204-2023 · Med-Mizer
Hazard
Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side. · FDA Class II
Units
241 units
Sold at
Awaiting consignee list from the recalling firm.
Description
Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side.
Product
Med-Riser MR600 Patient Lift
Manufacturer(s)
Med-Mizer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →