Stryker recalls S3 MedSurg Beds sold to homes, which are designed for hospitals. Home users may not follow healthcare instructions, risking injury.
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 S3 MedSurg Beds that were sold to homes instead of hospitals. These beds are designed for healthcare facilities and home users may not understand the safety instructions, which could lead to injury.
These beds are designed for hospital use only and require specific safety instructions from healthcare professionals. Home users may not follow these instructions properly, increasing the risk of injury.
Homeowners who purchased Stryker S3 MedSurg Beds for personal use are most at risk. Healthcare facilities that bought these beds for hospital use are not affected by this recall.
Check for model numbers 3002, part numbers 3002S3CUSTOM, 3002S3EX, or 3002S3PATRIOT. The serial numbers listed in the recall include 110715076 through 150615371.
Look for model numbers 3002, part numbers 3002S3CUSTOM, 3002S3EX, or 3002S3PATRIOT on the bed.
Ensure you understand the healthcare-specific safety instructions for use, as home users may not be trained to operate these beds safely.
Stryker recalled these beds because they were distributed to residential customers instead of healthcare facilities, and home users may not follow the safety instructions designed for healthcare professionals.
No, hospitals that purchased these beds for clinical use are not affected by this recall.
Check the model and serial numbers to see if your bed is recalled. If it is, review the healthcare-specific safety instructions carefully.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2214-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2214-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
