Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burns 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 that could cause tissue burns or electrical shock. This affects specific units with listed serial numbers and item numbers.
The bed lacks required electrical safety test values, which means it may not properly protect against electrical issues. This could lead to tissue burns or electrical shock during normal use, especially in medical settings where beds are frequently used.
Healthcare facilities using the ProCuity bed series model 3009 are most at risk. Patients and staff could experience tissue burns or electrical shock if the bed is used without proper electrical safety tests.
Check for the model number 3009 and item number 3009PX-LE-400 on the bed. Affected units have specific serial numbers listed in the recall notice.
Look for the serial numbers listed in the recall notice: 2105002838, 2105002832, 2202000312, and other specific numbers.
The ProCuity bed series model 3009 is missing electrical safety test values, which could cause tissue burns or electrical shock during use.
Check the bed's serial number against the list provided in the recall notice to see if it's affected. If it is, stop using it and contact Stryker for further instructions.
Yes, the missing electrical safety tests could lead to tissue burns or electrical shock, especially in medical settings where beds are used frequently.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0427-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0427-2024 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.
