Device recall
Z-2440-2021: COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the…
FDA device recall · Class II · Copan Italia
Key facts
| Recall number (Z-number) | Z-2440-2021 |
|---|---|
| Recall event | 88437 |
| Product | COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the following reference numbers REF:501CS01, Minitip, sterile Single Wrapped, Molded bp 80mm; REF: 20226, P/N 501CS01Q100, Minitip, Sterile, Single Wrapped, bp 60MM, BUNDLES OF 20 pcs; REF: 501CS01.Q20, P/N 1127700, Minitip… |
| Product code | KXG |
| Recalling firm | Copan Italia |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 25, 2024 |
| FEI number | 3002444944 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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