Stryker recalls Symmetry Plus Treatment Recliners sold to homes. These hospital-grade chairs may cause injury if used incorrectly in residential settings due to unmet safety requirements.
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 Symmetry Plus Treatment Recliners that were sold to homes instead of hospitals. These chairs are designed for healthcare facilities and may cause injury if used incorrectly in home environments where users might not follow proper safety instructions.
These chairs were designed for hospital use with specific safety requirements that home users may not follow. Without proper training and environment, they could tip over or cause injury due to incorrect usage.
Homeowners who purchased Symmetry Plus Treatment Recliners for personal use are most at risk. Healthcare facilities that used these chairs incorrectly for home settings may also face safety issues.
Check for model number 3500 or part number 3500000710. Look for serial numbers starting with G201170298, G201181816, or G201318385. The product was sold to residential customers instead of healthcare facilities.
Verify your Symmetry Plus Treatment Recliner has model number 3500 or part number 3500000710.
Ensure you follow the specific safety guidelines for healthcare facilities, as home use may be unsafe.
Stryker recalled these chairs because they were distributed to residential customers instead of healthcare facilities where they are designed to be used.
No, home use is not intended. These chairs are designed for healthcare facilities and may cause injury if used incorrectly in home environments.
Check your product details to confirm it's recalled. If it is, follow the safety instructions for healthcare facilities, as home use is unsafe.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2218-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2218-2021 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.
