Stryker recalls ProCuity bed model 3009 with missing electrical safety tests, risking tissue burns or 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 shock. This affects specific units with listed serial numbers and item numbers.
The beds lack required electrical safety test values, meaning they might not properly protect against electrical shocks or tissue burns during use. This could happen if the bed's electrical components fail under normal operating conditions.
Healthcare facilities using the ProCuity bed series model 3009 are most at risk. Patients and staff could be affected if the bed is used without proper electrical safety testing.
Check for the model number 3009 and item number 3009PX-LE-450 on the bed. Affected units have specific serial numbers listed in the recall notice.
Inspect the bed for missing electrical safety test values, which could indicate a risk of tissue burns or shock.
The model number is 3009.
Affected units have serial numbers: 2109000993, 2208000147, 2209000850, 2211002051, 2202000910, 2209000408, 2205000619, 2205000615, 2205000612, 2205000587, 2205000746, 2205000745, 2205000739, 2109000135, 2109000124.
Check for the model number 3009 and item number 3009PX-LE-450, and verify the serial number against the list provided in the recall notice.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0428-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0428-2024 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.
