Stryker recalls GoBed II MedSurg Beds (model FL28) sold to homes. These hospital-grade beds may cause injury if used outside healthcare settings without proper 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 GoBed II MedSurg Beds (model FL28) that were mistakenly sold to home users instead of healthcare facilities. These beds are designed for professional medical use and may cause injury if operated without proper training.
The bed is designed for healthcare facilities with specific training and protocols. Home users may not understand the proper setup, adjustments, or safety requirements that could lead to injury if used incorrectly.
Home users who purchased the GoBed II MedSurg Bed (model FL28) are affected. Healthcare professionals using the bed in a facility are not at risk as it was intended for that environment.
Check for model number FL28 on the bed or its packaging. Look for serial numbers listed in the recall: R52495, R53376, R55047, R56034, M14805, M14885, M14886, M14931, M14936, M14938, M14939, M50074, M50425, M50951, M50956, M54387, R63407, R54523, R54610, R54696, R54698, R60775, R32649, R25384, R35631, R35734, R58735, M15330, R58474.
Look for model number FL28 on the bed or its packaging to confirm it's in the recall list.
Reach out to Stryker for guidance on next steps if you have the recalled model.
The bed was designed for healthcare facilities and may be used incorrectly at home without proper training, posing a risk of injury.
No, this bed is intended for healthcare settings only. Home users should not operate it without professional training.
Check if your bed is in the recall list and 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-2223-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2223-2021 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.
