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FDA (Device enforcement)Recalled 2024-10-28class iii

Remote Diagnostic Technologies Ltd.: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode

Hazard

Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.

Details from the source

Reason for recall: Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number. Distribution: U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA. Lot/code info: Model Number: 00-3020 UDI-DI code: 07613365002737 Serial Numbers: 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

UPC codes

07613365002737

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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