FDA-Device2023-03-08Class II

Med-Riser MR600 Patient Lift

Med-Mizer, Inc.
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.

Sold states
Awaiting consignee list from the recalling firm.
Affected count
241 units
Manufactured in
80 Commerce Dr, N/A, Batesville, IN, United States
Products
Med-Riser MR600 Patient Lift

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1204-2023

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief