Stryker recalls CUB Pediatric Crib devices sold to homes, which were intended for healthcare facilities. Home users may not understand proper use, 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 CUB Pediatric Crib devices that were mistakenly sold to homes instead of healthcare facilities. These cribs are designed for medical use in hospitals and home users may not understand how to safely operate them, potentially causing injury.
The crib was designed for healthcare facilities and requires specific professional training. Home users may not understand the correct use instructions, which could lead to improper handling and injury.
Home users who purchased the CUB Pediatric Crib for non-medical purposes are most at risk. Healthcare facilities that received the product for medical use are not affected by this recall.
Check for model number FL19, part number 5050000000, or serial numbers F09519 and F50699. The product was sold to residential customers, not healthcare facilities.
Identify the model number (FL19), part number (5050000000), or serial numbers (F09519, F50699) to confirm if your crib is recalled.
Reach out to Stryker directly for guidance on whether your crib is affected and what to do next.
The crib was designed for healthcare facilities and was mistakenly sold to residential customers. Home users may not understand the proper use instructions intended for healthcare professionals.
No, the crib is intended for healthcare facilities only and home use without proper training could lead to injury.
Check the product details to confirm if it's recalled, then contact Stryker for guidance on next steps.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2221-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2221-2021 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.
