Spacelabs Healthcare recalls SL Command Module software version 91496 due to potential electrical leakage. Affected units may cause electrical hazards; contact Spacelabs for details.
Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).
Spacelabs Healthcare is recalling the SL Command Module software version 91496 because of a manufacturing issue that could cause electrical leakage. This poses a risk of electrical hazards, especially in medical settings where the device is used for patient monitoring.
The device has a manufacturing issue causing potential electrical leakage. This could lead to electrical hazards, but the risk is low as it's a software issue and not a physical defect that causes immediate danger.
Healthcare facilities using Spacelabs patient monitors with the SL Command Module model 91496 are most at risk. Patients and staff in hospitals or clinics using this specific device may be affected.
Check if your Spacelabs patient monitor has the SL Command Module model 91496. Look for serial numbers starting with 1496-224657 to 1496-224716.
Verify your Spacelabs patient monitor has the SL Command Module model 91496 with serial numbers listed in the recall.
Reach out to Spacelabs Healthcare for specific guidance on next steps if you have the affected model.
The recall states there is a potential for electrical leakage due to a manufacturing issue, but the risk is low and not immediately dangerous.
Check for the SL Command Module model 91496 with serial numbers starting from 1496-224657 to 1496-224716.
The recall does not specify a need to stop using the device immediately; contact Spacelabs for further instructions.
We’ve drafted a message you can send Spacelabs to request your refund or repair — edit it as you like.
Subject: Recall Z-2052-2026 — Spacelabs Spacelabs Hello, I own a Spacelabs that is covered by recall Z-2052-2026 from Spacelabs. 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.
