Philips Medical Systems Gmbh, DMC recalls DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
- Recall date
- June 27, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2849-2018
- FDA classification
- Class II
- Brand / firm
- Philips Medical Systems Gmbh, DMC
- Sold / distributed
- US Nationwide; International to 66 countries
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
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