Device recall event
Recall event 80928: GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
FDA device recall · Class II · Terminated
Key facts
| Recall event number | 80928 |
|---|---|
| Recalling firm | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
| Recall class | Class II |
| Status | Terminated |
| 510(k) numbers | K060542, K061129, K082185, K092271, K110943, K123564, K131514, K142160, K150087, K170823, K173341 |
At a glance
- 1–9 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