Device recall
Z-1120-2022: Outer Packaging Label: Protekt Sharps Safety Knives - REF: PG 44620MU, Sterile…
FDA device recall · Class II · International Science & Technology, LP, DBA Diamatrix Ltd.
Key facts
| Recall number (Z-number) | Z-1120-2022 |
|---|---|
| Recall event | 89827 |
| Product | Outer Packaging Label: Protekt Sharps Safety Knives - REF: PG 44620MU, Sterile R, Multi-Use 2.2mm Double Bevel Slit, Angled 6 units, Individual Packaging Label: ProTekt Sharps Safety Knives - REF: PG 44620MU,2.2mm double Bevel Slit, Sterile R, Angled 1 unit, Handle Labeling; 2.5mm slit double bevel |
| Product code | HNN |
| Recalling firm | International Science & Technology, LP, DBA Diamatrix Ltd. |
| Recall class | Class II |
| Status | Completed |
| FEI number | 3000892087 |
At a glance
- None 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