Stryker recalls ProCurity bed model 3009 with missing electrical safety test values that could cause electrical shock or tissue burns. 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 ProCurity bed series model 3009 due to missing electrical safety test values, which could lead to electrical shock or tissue burns. This recall 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 shocks or burns during use. This could happen if the bed is used in a medical setting where electrical safety is critical.
Healthcare facilities using the ProCurity bed series model 3009 are most at risk. Patients and staff could be affected if the bed is used without proper electrical safety checks.
Check for the model number 3009 and item number 3009PX-ZMX-600 on the bed. Affected units have specific serial numbers listed in the recall notice.
Inspect the bed for any signs of electrical damage or unusual heat, but note that the recall is based on missing test values, not visible damage.
Reach out to Stryker directly to confirm if your specific bed model and serial number are affected by this recall.
The bed lacks required electrical safety test values, which could lead to electrical shock or tissue burns during use.
Check your bed's model number and serial number against the list provided in the recall notice. Contact Stryker for confirmation.
The recall record does not mention a remedy or fix, so no immediate action is required beyond checking if your unit is affected.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0435-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0435-2024 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.
