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 specific units with listed serial numbers and item numbers.
The beds lack required electrical safety test values, which means they might not properly prevent electrical shocks or burns. This could happen during normal use when the bed is operating, especially if the electrical system is faulty.
Healthcare facilities using the ProCuity bed series model 3009 are most at risk. Patients and staff using these beds could be affected if the electrical safety tests are missing.
Check for the model number 3009 and item number 3009PX-LEX-400 on the bed. Affected units have specific serial numbers listed in the recall notice.
Look for the model number 3009 and item number 3009PX-LEX-400 on the bed. Affected units have specific serial numbers listed in the recall notice.
The beds are missing test values for electrical safety tests, which could lead to tissue burns or electrical shocks.
Check the model number and item number on the bed. If it matches the recalled model 3009 with item number 3009PX-LEX-400, contact Stryker for further instructions.
Yes, the recall includes specific serial numbers listed in the notice, such as 2203001674, 2203001673, and others.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0429-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0429-2024 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.
