Device recall
Z-1945-2018: Symmetry Olsen monopolar forceps: (a) Insulated Potts-Smith Forceps 8" (20.3cm)…
FDA device recall · Class II · Olsen Medical
Key facts
| Recall number (Z-number) | Z-1945-2018 |
|---|---|
| Recall event | 80080 |
| Product | Symmetry Olsen monopolar forceps: (a) Insulated Potts-Smith Forceps 8" (20.3cm) Serrated Tips, REF 20-2650K, QTY 10 (b) Insulated Bayonet Forceps 8.25" (21.0cm) Serrated 1.5mm Tips, REF 20-2920HK, QTY 10 (c) Insulated Bayonet Forceps 8.5" (21.6cm) Serrated 1.5mm Tips, REF 20-2920K, QTY 10 (d)… |
| Product code | GEI |
| Recalling firm | Olsen Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2019 |
| 510(k) numbers | K080187 |
| FEI number | 3000719969 |
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