Stryker recalls TruRize Clinical Chairs sold to homes. These medical chairs are designed for healthcare facilities but may be used at home without proper understanding of safety instructions.
Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately identifies the correct use environment, but home users may not be aware of or fully understand these instructions intended for healthcare professionals
Stryker is recalling TruRize Clinical Chairs that were sold to residential customers. These chairs are designed for healthcare facilities but may be used at home without proper understanding of safety instructions, which could lead to injury.
The chairs are designed for healthcare settings with specific safety instructions. Home users may not be aware of or understand these instructions, potentially leading to improper use and injury.
Home users who purchased the TruRize Clinical Chair for personal use are most at risk. Healthcare facilities that used the chair without proper training may also be affected.
Check for model number 3333 and serial numbers starting with 2017000300284. The chairs were sold to residential customers, not healthcare facilities.
Look for model number 3333 and serial numbers starting with 2017000300284 on the chair.
The chairs were distributed to residential customers but are designed for healthcare facilities. Home users may not understand the safety instructions intended for healthcare professionals.
No, the chairs are designed for healthcare settings with specific safety instructions. Home users may not be aware of or understand these instructions.
Check the model number and serial numbers to confirm if it's recalled. The recall does not specify a remedy, so contact Stryker for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2217-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2217-2021 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.
