Philips Medical Systems North America Inc.: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: November 27, 2013. Most recent: March 26, 2014.
Risk classification: Class II: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| March 26, 2014 | FDA | Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Pr…Z-1232-2014 | Z-1232-2014 |
| March 26, 2014 | FDA | Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. …Z-1225-2014 | Z-1225-2014 |
| March 26, 2014 | FDA | Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound imaging and f…Z-1264-2014 | Z-1264-2014 |
| March 26, 2014 | FDA | Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound imaging and f…Z-1263-2014 | Z-1263-2014 |
| November 27, 2013 | FDA | EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultras…Z-0368-2014 | Z-0368-2014 |
Questions about this company
- How many recalls does Philips Medical Systems North America Inc. have?
- Recalert has 5 U.S. recalls on record for Philips Medical Systems North America Inc., published between November 27, 2013 and March 26, 2014.
- What was the most recent Philips Medical Systems North America Inc. recall?
- FDA recall Z-1232-2014, published March 26, 2014: Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product Usage: The models M5066A, M5067A, and M5068A are designed for use on a person in sudden cardiac arrest …
- Which agencies have handled Philips Medical Systems North America Inc. recalls?
- Philips Medical Systems North America Inc. appears as the recalling firm in recalls from: FDA (5).
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