Stryker recalls Prime Big Wheel Stretcher (Model 1115) for home use. Healthcare devices distributed to residential customers may cause injury if misused without professional training.
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 its Prime Big Wheel Stretcher (Model 1115) because it was sold to home users instead of healthcare facilities. This device is designed for clinical use only and home users may not understand the risks without professional training.
This medical device is intended for use in healthcare facilities only. Home users may not have the training or environment to safely operate it, increasing the risk of injury from improper use.
Home users who purchased this stretcher for personal use are most at risk. Healthcare professionals who used it in clinical settings are not affected by this recall.
Check for the model number 1115 on the stretcher. The product was distributed to residential customers and may be in home environments.
Look for the model number 1115 on the stretcher to confirm it is recalled.
No, this stretcher is designed for healthcare facilities only and not for home use.
The recall states that medical devices were distributed to residential customers by mistake.
Check the model number 1115 to confirm it is recalled; if so, stop using it and 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-2208-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2208-2021 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.
