Stryker recalls ProCuity bed model 3009 (item 3009PX-ZM-600) due to missing electrical safety test values that could cause tissue burns or electrical shock. Affected units have specific serial numbers and UDI-DI codes.
Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
Stryker is recalling ProCuity bed model 3009 (item number 3009PX-ZM-600) because electrical safety tests are missing, which could lead to tissue burns or electrical shock. This affects specific units with listed serial numbers and UDI-DI codes.
The beds lack required electrical safety test values, meaning they might not properly protect against electrical issues. This could cause tissue burns or electrical shock during normal use, especially in medical settings.
Patients using hospital beds with the recalled model number 3009 are at risk. Healthcare facilities that own these beds should check if their units are affected.
Check for the model number 3009 and item number 3009PX-ZM-600 on the bed. Affected units have specific serial numbers listed in the recall notice, including 2201000173 and others.
Look for the model number 3009 and item number 3009PX-ZM-600 on the bed's label.
Reach out to Stryker directly to confirm if your bed is affected using the provided serial numbers or UDI-DI code.
The beds are missing electrical safety test values, which could cause tissue burns or electrical shock during normal use.
Check for the model number 3009 and item number 3009PX-ZM-600. Affected units have specific serial numbers listed in the recall notice.
Contact Stryker directly to confirm if your bed is affected using the provided serial numbers or UDI-DI code.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0433-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0433-2024 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.
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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.
