Stryker recalls Prime Fifth Wheel Stretcher model 1105 for home use. The device is intended for healthcare facilities but may be used at home without proper training, 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 its Prime Fifth Wheel Stretcher model 1105 because it was distributed to residential customers instead of healthcare facilities. Home users may not understand the proper use instructions intended for healthcare professionals, which could lead to injury.
The stretcher is designed for healthcare facilities and requires professional training. Home users may not understand the instructions, which could lead to improper use and injury.
Home users who own the Prime Fifth Wheel Stretcher model 1105 are most at risk. Healthcare facilities were not intended to use this device, so home users may not be aware of the proper training needed.
Check for model number 1105 and part numbers 1105000026 or 1105000000X. The device was sold to residential customers, not healthcare facilities.
Identify the model number and part numbers to confirm if your stretcher is affected.
Reach out to Stryker for guidance on next steps if you have the affected model.
No, the stretcher is intended for healthcare facilities only and requires professional training. Home users may not understand the proper use instructions.
Check the model number and part numbers to confirm if it's affected. Contact Stryker for guidance on next steps.
The recall record states that the device was distributed to residential customers instead of healthcare facilities, which is not its intended use environment.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2207-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2207-2021 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.
