Device recall
Z-1375-2021: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by…
FDA device recall · Class I · Pacific Medical Group Inc.
Key facts
| Recall number (Z-number) | Z-1375-2021 |
|---|---|
| Recall event | 87483 |
| Product | Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel, installed by Pacific Medical Group (DBA Avante Health Solutions) |
| Product code | FRN |
| Recalling firm | Pacific Medical Group Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K133532 |
| FEI number | 3007409280 |
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