Remote Diagnostic Technologies Ltd.: Tempus LS-Manual Defibrillator Model
Recall reason: Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.. Recalled by Remote Diagnostic Technologies Ltd.. Distribution: U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.. Classification (Class III — minor violation). Affected lots/dates: Model Number: 00-3020 UDI-DI code: 07613365002737 Serial Numbers: 7022.000367 7022.000387 7022.000392 7022.000462 7022.0. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.
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