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Mizuho OSI recalls Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: in
Recalled March 31, 2021 · FDA recall Z-1293-2021 · Mizuho OSI
Hazard
There is a potential that hand control units may cause the tabletop to slide in the opposite direction from that selected by the user. This could result in a delay in procedure. · FDA Class II
Units
26 units
Sold at
Worldwide distribution - US Nationwide distribution in the state of CA, and the countries of Costa Rica, Chile, Bolivia, Peru.
Description
There is a potential that hand control units may cause the tabletop to slide in the opposite direction from that selected by the user. This could result in a delay in procedure.
Product
Mizuho CE IPX4, mode MOT-5602BW, 100-240, 50-60Hz, 400VA, REF 18-140-20 containing hand control Unit - Product Usage: intended to support a patient during surgical operations.
Manufacturer(s)
Mizuho OSI
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →