Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1825-2023 — Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020

U.S. FDA — Device Enforcement · United Kingdom · 2023-05-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1825-2023
Date of alert
2023-05-08
Country / jurisdiction
United Kingdom
Risk level
Class II
Risk type
recall
Brand
Remote Diagnostic Technologies Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07613365002737
Reported risk: Defibrillator/pacemaker module (DPM) may encounter a problem causing communication from the Mainboard to the DPM to fail, leading to no or ineffective pacing with displayed error message "HW failure DPM".
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.