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FDAOctober 28, 2024device

Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

remote diagnostic technologiesremoteremote diagnostic

UPCs

07613365002737

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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