FDA recall record

Remote Diagnostic Technologies Tempus LS-Manual Defibrillator Model 00-3020 The Tempus recall — FDA Z-0557-2025

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

Class IIIclassification
Z-0557-2025official record ID
Dec 4, 2024report date

Recall record at a glance

Official recordZ-0557-2025
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmRemote Diagnostic Technologies Ltd.
Report dateDec 4, 2024
Recall initiation dateOct 28, 2024
LocationFarnborough, United Kingdom

Official product description

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

Why the product was recalled

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

Distribution information

U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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