Philips Tempus LS-Manual Defibrillator recall
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Why was Philips Tempus LS-Manual Defibrillator recalled?
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".
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 07613365002737. Serial numbers prior to 7022.001634
- Product
- Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
- Recalling firm
- Remote Diagnostic Technologies Ltd.
- Quantity
- 1147
- Distribution
- US Nationwide distribution in the states of UT, CO, CA, NE, IL, TX, WV, KS, GA.
- Recall date
- June 21, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)