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symbio-cart

ITD GmbH · Model KN.1517.800 · UDI-DI 04056634076856

BZN
8
510(k) clearances
141
Adverse events (1 deaths)
2
Recalls
134
Facilities

Description

symbio-cart B450 30/35E

Recalls

DateFirmReason
2019-04-23Stryker CorporationThere is a potential problem with firm s Connected OR Cart, 120V resulting in cart monitor not attaching flush with their monitor stow handle. The product is not manufactured to sp
2013-08-30Stryker EndoscopyWhen positioning the display located on top of the video cart, it is possible for the user to apply excessive force and push the display up and out of the mounting arm. This can re

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.