Device recall
Z-0456-2019: Powdered Surgical Gloves, labeled as: a. Baxter and Ansell brand Powdered…
FDA device recall · Class II · American Contract Systems, Inc.
Key facts
| Recall number (Z-number) | Z-0456-2019 |
|---|---|
| Recall event | 80754 |
| Product | Powdered Surgical Gloves, labeled as: a. Baxter and Ansell brand Powdered Surgical Gloves b. Powdered Surgical Gloves included in ACS surgical convenience kits Health care personnel rely on medical gloves as barriers against transmission of infectious diseases and contaminants when conducting… |
| Product code | KGO |
| Recalling firm | American Contract Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 14, 2018 |
| FEI number | 3003419114 |
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