Device recall
Z-1474-2020: CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG…
FDA device recall · Class I · CME America, LLC
Key facts
| Recall number (Z-number) | Z-1474-2020 |
|---|---|
| Recall event | 85033 |
| Product | CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and CMExpress |
| Product code | FRN |
| Recalling firm | CME America, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 14, 2022 |
| 510(k) numbers | K061325 |
| FEI number | 3006967710 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database