Device recall event
Recall event 79813: Tosoh Bioscience Inc
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 79813 |
|---|---|
| Recalling firm | Tosoh Bioscience Inc |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K010796, K012820, K023091, K023240, K023893, K023894, K093960, K143075, K863345, K863861, K870521, K913298 and 5 more |
| PMA numbers | P910065 |
At a glance
- 10–99 Recalled products (Z-numbers)
- 10–99 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