Reported Dec 4, 2024 · Ongoing
Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual…
Remote Diagnostic Technologies Ltd.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Remote Diagnostic Technologies Ltd. · Farnborough Aerospace Centre · Farnborough · N/A
Is this the product you have?
- Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or Pacemaker mode
- Lot codes and dates
- Model Number00-3020
- UDI-DI code07613365002737
- Serial Numbers
7022.0003677022.0003877022.0003927022.0004627022.0004637022.0004647022.0005597022.0005917022.0005957022.0007117022.0007817022.0007867022.001087022.0011757022.0012017022.001297022.0015567022.001582
Where it was sold
Why it was recalled
Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
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