Device recall
Z-0365-2020: Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN…
FDA device recall · Class II · Cadence Science, Inc.
Key facts
| Recall number (Z-number) | Z-0365-2020 |
|---|---|
| Recall event | 83867 |
| Product | Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use |
| Product code | FMF |
| Recalling firm | Cadence Science, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 5, 2020 |
| FEI number | 1213649 |
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