Remote Diagnostic Technologies recalls Tempus LS-Manual Defibrillator Model 00-3020 due to incorrect labels during servicing. Labels have wrong product names and CAT numbers, potentially causing misidentification. Affected units have specific serial numbers.
Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.
Remote Diagnostic Technologies is recalling Tempus LS-Manual Defibrillators with model number 00-3020 because labels during servicing contain incorrect product names and CAT numbers. This could lead to misidentification of the device, which might cause confusion in medical settings.
Incorrect labels during servicing show the wrong product name and CAT number. This could lead to confusion about which defibrillator is being used, potentially causing misidentification in medical settings.
Healthcare professionals using the Tempus LS-Manual Defibrillator Model 00-3020 are most at risk. Patients receiving care from these devices could be affected if misidentified.
Check for the model number 00-3020 on the device. Look for specific serial numbers listed: 7022.000367, 7022.000387, 7022.000392, 7022.000462, 7022.000463, 7022.000464, 7022.000559, 7022.000591, 7022.000595, 7022.000711, 7022.000781, 7022.000786, 7022.00108, 7022.001175, 7022.001201, 7022.00129, 7022.001556, 7022.001582.
Look for incorrect product names or CAT numbers on the device labels.
The model number is 00-3020.
Check for the specific serial numbers listed: 7022.000367, 7022.000387, 7022.000392, 7022.000462, 7022.000463, 7022.000464, 7022.000559, 7022.000591, 7022.000595, 7022.000711, 7022.000781, 7022.000786, 7022.00108, 7022.001175, 7022.001201, 7022.00129, 7022.001556, 7022.001582.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
We’ve drafted a message you can send Remote Diagnostic Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0557-2025 — Remote Diagnostic Technologies Remote Diagnostic Technologies Hello, I own a Remote Diagnostic Technologies that is covered by recall Z-0557-2025 from Remote Diagnostic Technologies. 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.
