Device recall
Z-0521-2020: ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium…
FDA device recall · Class II · Zimmer Biomet, Inc.
Key facts
| Recall number (Z-number) | Z-0521-2020 |
|---|---|
| Recall event | 83783 |
| Product | ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium replacement. |
| Recalling firm | Zimmer Biomet, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 21, 2021 |
| FEI number | 1825034 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 1–9 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