Stryker recalls Michael Graves Highback Chairs (Model 4853) sold to homes. These 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 Michael Graves Highback Chairs (Model 4853) that were sold to home users. These chairs are intended for healthcare facilities, not homes, and home users may not understand the safety instructions meant for healthcare professionals.
The chairs are designed for indoor medical settings with specific safety instructions for healthcare professionals. Home users may not be aware of or understand these instructions, potentially leading to unsafe use.
Home users who purchased the Michael Graves Highback Chair (Model 4853) for seating. People who use the chair in home settings without proper healthcare training are at higher risk.
Check for the model number 4853 on the chair. Look for serial numbers starting with G201179538 or UDI 07613327506129. These chairs were sold to residential customers, not healthcare facilities.
Look for the model number 4853 and serial numbers starting with G201179538 or UDI 07613327506129.
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.
Check the product label for the model number 4853 and serial numbers. If you have the chair, you may need to contact Stryker for guidance on safe use.
The recall record does not specify a remedy or fix. You should check with 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-2219-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2219-2021 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.
