Stryker recalls ProCuity bed series model 3009 with missing electrical safety test values, risking tissue burn or electrical shock. Affected units have specific serial numbers listed.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Stryker is recalling ProCuity bed series model 3009 due to missing electrical safety test values, which could cause tissue burns or electrical shocks. This affects specific units with listed serial numbers.
The beds lack required electrical safety test values, meaning they might not properly protect against electrical faults. This could lead to electrical shocks or tissue burns if the bed malfunctions during use.
Healthcare facilities using the ProCuity bed series model 3009 are most at risk. Patients and staff using these beds could face injury if the electrical safety issues are not addressed.
Check if your bed has the model number 3009 and the listed serial numbers in the description. The item number is 300900000000.
Review the list of affected serial numbers provided in the recall notice to determine if your bed is included.
The ProCuity bed series model 3009 is missing electrical safety test values, which could cause tissue burns or electrical shocks.
Check if your bed has the model number 3009 and a serial number from the list provided in the recall notice.
The recall notice does not specify a remedy, so contact Stryker directly 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-0424-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0424-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
