Device recall
Z-0683-2020: A1CNow SELF CHECK (European), Software Version Revision D, REF Numbers 3054…
FDA device recall · Class II · Polymer Technology Systems
Key facts
| Recall number (Z-number) | Z-0683-2020 |
|---|---|
| Recall event | 84231 |
| Product | A1CNow SELF CHECK (European), Software Version Revision D, REF Numbers 3054, 3062 |
| Product code | LCP |
| Recalling firm | Polymer Technology Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 16, 2020 |
| 510(k) numbers | K090413 |
| FEI number | 3002698769 |
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