Device recall event
Recall event 91863: AGILENT TECHNOLOGIES INC./US
FDA device recall · Class III · Open, Classified
Key facts
| Recall event number | 91863 |
|---|---|
| Recalling firm | AGILENT TECHNOLOGIES INC./US |
| Recall class | Class III |
| Status | Open, Classified |
| PMA numbers | P210040, P210040/A005, P210040/A006 |
At a glance
- 1–9 Recalled products (Z-numbers)
- None 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