Philips HeartStart XL+ Defibrillator/Monitor recall
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Why was Philips HeartStart XL+ Defibrillator/Monitor recalled?
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
Serial Numbers: USN1307680 USD1309181 USD1308456 USD1309182 USD1309167 USD1309184 USD1309168 USD1309194 USD1309180 USD1309195 USD1309196 USD1309274 USD1309197 USD1309286 USD1309227 USD1309301 USD1309264 US11409686 USD1309269
- Product
- Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
- Recalling firm
- Philips Medical Systems, Inc.
- Quantity
- 19 units
- Distribution
- Worldwide Distribution - US Distribution including the states of IN and WA., and the countries of : CHINA FRANCE GERMANY ITALY MALAYSIA PANAMA SAUDI ARABIA TURKEY and UNITED KINGDOM.
- Recall date
- April 16, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)