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ITD

Touchpoint Medical, Inc. · Model TP.5003.999 · UDI-DI 00840178700179

BZN

510(k) clearances

140

Adverse events (1 deaths)

Recalls

134

Facilities

Description

ENDO CART w/ CROSS BAR and TRANSFORMER, 30U+10U, 1100W, SYMMETRICAL w PACKAGING

Recalls

Date	Firm	Reason
2019-04-23	Stryker Corporation	There 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
2013-08-30	Stryker Endoscopy	When 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.