Device recall event
Recall event 60737: Sorin Group USA, Inc.
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 60737 |
|---|---|
| Recalling firm | Sorin Group USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K014080, K020997, K032040, K033323, K043323, K050447, K073380, K083021, K092895 |
At a glance
- 10–99 Recalled products (Z-numbers)
- 1–9 Linked 510(k)s
- 10–99 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