Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burn or electrical shock. Affected units have specific serial numbers and item numbers.
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 medical beds used in hospitals and clinics.
The beds lack required electrical safety test values, which could lead to electrical shocks or tissue burns if the bed is used improperly. This is a safety issue specific to medical equipment that handles patients.
Healthcare facilities using the ProCuity bed series model 3009 are most at risk. Patients and staff in hospitals and clinics that own or use these beds may be affected.
Check for the model number 3009 and item number 3009PX-LEX-450 on the bed. Affected units have specific serial numbers listed in the recall notice.
Look for the serial numbers listed in the recall notice (e.g., 2207000806, 2101001244) on the bed's label.
Reach out to Stryker Medical Division at 1-800-442-2222 for specific instructions on whether your bed is affected.
The ProCuity bed series model 3009 has missing electrical safety test values, which could cause tissue burns or electrical shocks during use.
Check for the model number 3009 and item number 3009PX-LEX-450, and look for the specific serial numbers listed in the recall notice.
Contact Stryker Medical Division at 1-800-442-2222 for instructions on whether your bed needs repair or replacement.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0430-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0430-2024 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.
