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 home users instead of hospitals. These beds are designed for clinical settings and home use could lead to injury if not used correctly.
The beds are designed for hospital use with specific instructions for healthcare professionals. Home users may not follow these instructions, increasing the risk of injury.
Home users who own S3 MedSurg Beds intended for hospitals are affected. Those with medical conditions or limited understanding of healthcare procedures are at higher risk.
Check for model number 3005, part number 3005S3EX, or serial numbers starting with 120916611, 121016000, 130115957, or 130815166.
Verify the model number (3005), part number (3005S3EX), or serial numbers listed in the recall notice.
The beds were distributed to residential customers instead of hospitals, where they are designed to be used. Home users may not follow healthcare instructions.
Check for model number 3005, part number 3005S3EX, or serial numbers starting with 120916611, 121016000, 130115957, or 130815166.
The recall notice does not specify a remedy, so contact Stryker directly 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-2216-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2216-2021 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.
