Stryker recalls Isolibrium Support Surfaces sold to homes. These medical-grade products are intended for healthcare facilities only. Home users may not understand proper use, risking pressure injuries.
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 Isolibrium Support Surfaces that were sold to home users. These medical devices are designed for healthcare facilities, not homes. Home use could lead to pressure injuries if not used correctly.
These medical-grade surfaces are designed for healthcare facilities with trained staff. Home users may not understand the correct use instructions, increasing the risk of pressure injuries.
Home users who purchased Isolibrium Support Surfaces for pressure injury treatment. Healthcare professionals are not affected as the product is intended for clinical settings.
Check for model number 2972 or serial numbers starting with 219009000417. The product was sold to residential customers, not healthcare facilities.
Look for model number 2972 or serial numbers starting with 219009000417 on the product.
Reach out to Stryker for guidance on whether the product is safe for home use.
No, these medical devices are intended for healthcare facilities only. Home users may not understand the proper use instructions.
Check the product label for model number 2972 or serial numbers starting with 219009000417. Contact Stryker for guidance.
Stryker states the product is not designed for home use. Home users may not understand the instructions, risking pressure injuries.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2215-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2215-2021 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.
