Stryker recalls FL23 hospital beds sold to homes due to improper use instructions. Home users may not understand healthcare-specific 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 electric hospital beds (FL23 model) that were sold to homes. These beds are designed for healthcare facilities, but home users may not understand the safety instructions meant for medical professionals.
The bed was designed for healthcare facilities with specific safety instructions. Home users may not understand these instructions, which could lead to improper use. This could result in injury if the bed is not used correctly in a home environment.
Home users of the Stryker FL23 hospital bed who may not be aware of the healthcare-specific safety requirements. Healthcare facilities that purchased these beds for home use are also affected.
Check for the model number FL23 on the bed's label. The serial numbers listed in the recall include FL23J50576 through FL23J60627 and J29770 through J32350.
Look for the model number FL23 on the bed's label to confirm if it's recalled.
Ensure you understand the healthcare-specific safety instructions for proper use in a home environment.
The bed was designed for healthcare facilities but sold to residential customers. Home users may not understand the healthcare-specific safety instructions.
Check for the model number FL23 on the bed's label. The serial numbers listed in the recall include FL23J50576 through FL23J60627 and J29770 through J32350.
No, but you must understand the healthcare-specific safety instructions for home use to avoid injury.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2222-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2222-2021 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.
