Medical Device Recalls
-
|
1 to 10 of 27 Results
510(K) Number: K030455 |
Results per Page |
|
Product Description
![Sort by Product Name [A-Z]](/scripts/cdrh/images/arrow_up-black.GIF){kind=icon} ![Sort by Product Name [Z-A]](/scripts/cdrh/images/arrow_down-black.GIF){kind=icon}
|
Recall
Class
|
FDA Recall
Posting Date
|
Recalling Firm
|
|---|---|---|---|
| iE33 Ultrasound System (System, imaging, pulsed doppler, ultrasonic and system, imaging, pulsed echo... | 2 | 02/17/2007 | Philips Ultrasound, Inc. |
| L8-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| L9-3 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| TRANSDUCER L12-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C5-2 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-4v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-4v Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C8-5 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-4 Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
| C9-5ec Transducer Probe | 3 | 08/22/2025 | Philips Ultrasound, Inc |
-
