Device recall event
Recall event 96994: Philips Ultrasound, Inc
FDA device recall · Class II · Open, Classified
Key facts
| Recall event number | 96994 |
|---|---|
| Recalling firm | Philips Ultrasound, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K030455, K042540, K043535, K062247, K081661, K081802, K091804, K111513, K120321, K123754, K130499, K132304 and 10 more |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 Linked 510(k)s
- 1–9 Recall events for this firm
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall events
A recall event groups every recalled product (Z-number) from one recall action by a firm. Class I recalls involve a reasonable probability of serious harm; Class III recalls are unlikely to cause harm.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database