Reported Mar 8, 2023 · Ongoing
Med-Riser MR600 Patient Lift
Med-Mizer, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Med-Mizer, Inc. · 80 Commerce Dr · Batesville, IN · 47006-6700
Is this the product you have?
- Med-Riser MR600 Patient Lift
- Lot codes and dates
- UDI-DI
242 of 242 codes
00852195007308Serial No.: MR600000MR600001MR600002MR600003MR600004MR600005MR600006MR600007MR600008MR600009MR600010MR600011MR600012MR600013MR600014MR600015MR600016MR600017MR600018MR600019MR600020MR600021MR600022MR600023MR600024MR600025MR600026MR600027MR600028MR600029MR600030MR600031MR600032MR600033MR600034MR600035MR600036MR600037MR600038MR600039MR600040MR600041MR600042MR600043MR600044MR600045MR600046MR600047MR600048MR600049MR600050MR600051MR600052MR600053MR600054MR600055MR600056MR600057MR600058
- UDI-DI
- Amount recalled
- 241 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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