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Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
Recalled August 29, 2018 · FDA recall Z-2854-2018 · Philips Medical Systems Gmbh, DMC
Hazard
The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient. · FDA Class II
Sold at
US Nationwide; International to 66 countries
Description
The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.
Product
DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
Manufacturer(s)
Philips Medical Systems Gmbh, DMC
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →