Stryker recalls a specific medical cart model due to a risk of monitor falling from the cart, potentially causing injury. Affected units have a unique serial number and were sold in 2019.
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 specifications and is positioned on the incorrect side that may lead to monitor falling from the monitor arm and a risk of user injury.
Stryker is recalling a specific medical cart model that may not attach properly to its monitor handle. This could cause the monitor to fall during use, posing a risk of injury to the user.
The cart is manufactured incorrectly and may attach to the monitor handle on the wrong side. This positioning could cause the monitor to fall from the cart during use, potentially leading to injury.
Medical professionals using the Stryker Connected OR Cart for imaging procedures are most at risk. The recall affects specific units sold in 2019 with unique serial numbers.
Check for the model number 240-099-155 on the cart. Affected units have serial numbers starting with 2019AN and were sold in 2019.
Look for serial numbers starting with 2019AN on the cart to determine if it is affected.
Reach out to Stryker Corporation at 5900 Optical Court, San Jose, CA 95138 for specific recall information.
The cart is manufactured incorrectly and may attach to the monitor handle on the wrong side, causing the monitor to fall during use and potentially leading to injury.
Check the cart's serial number to see if it starts with 2019AN. If affected, contact Stryker Corporation for further instructions.
The recall record does not specify a fix or remedy for this issue.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1445-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1445-2020 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
