Stryker recalls ProCuity bed model 3009 with missing electrical safety test values, risking tissue burn or electrical shock during use.
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 shocks. This affects hospital beds used for patient care.
The bed lacks required electrical safety test values, which could lead to electrical shocks or tissue burns if the bed is used normally. This is a safety issue that requires immediate attention but does not require immediate discontinuation of use.
Hospital staff and patients using the ProCuity bed series model 3009 are most at risk. The recall affects beds sold in the U.S. with specific serial numbers.
Check for the model number 3009 and serial number starting with 2110001715 on the bed. The UDI-DI (GTIN) is 07613327541250.
Inspect the bed for missing electrical safety test values that could cause shocks or burns.
Yes, the bed may cause tissue burns or electrical shocks due to missing electrical safety test values.
Look for model number 3009 and serial number starting with 2110001715 on the bed.
Check for missing electrical safety test values and contact Stryker for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0431-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0431-2024 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.
