Lifepak 20e recall
LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
Why was Lifepak 20e recalled?
Incorrect keypad was incorrectly installed onto a defibrillator/monitor.
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?
Model/Catalog Number: 99507-000001 UDI-DI code: 00883873813751 Serial Number: 38289467
- Product
- LIFEPAK 20e REF 99507-000001 The AED mode is to be used only on patients in cardiopulmonary arrest.
- Recalling firm
- Physio-Control, Inc.
- Quantity
- 1
- Distribution
- U.S.: WV O.U.S.: N/A
- Recall date
- March 5, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)