Stryker recalls Prime TC transport chairs sold to homes, which were intended for healthcare facilities. Home users may not follow proper safety instructions for medical use.
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 Prime TC transport chairs that were sold to home users instead of healthcare facilities. These chairs are designed for medical settings and home users may not understand the safety instructions intended for healthcare professionals.
These chairs were designed for healthcare professionals in medical facilities, not for home use. Home users may not follow the safety instructions that healthcare professionals are trained to follow, increasing the risk of injury.
Home users who purchased the Prime TC transport chairs for personal use are most at risk. Healthcare facilities were not intended to use these chairs.
Check for model number 1460 or serial numbers starting with 1911040132 or 1911040133. The chairs were sold to residential customers instead of healthcare facilities.
Look for model number 1460 or serial numbers starting with 1911040132 or 1911040133 on the chair.
The chairs were designed for healthcare facilities, not home use. Home users may not understand the safety instructions intended for healthcare professionals.
No, these chairs were intended for medical facilities only. Home users may not follow the safety instructions properly.
Check the model number and serial numbers to see if your chair is affected. If it is, contact Stryker for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2209-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2209-2021 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.
