Device recall
Z-1227-2015: Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps…
FDA device recall · Class II · Baxter Corporation Englewood
Key facts
| Recall number (Z-number) | Z-1227-2015 |
|---|---|
| Recall event | 70128 |
| Product | Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100… |
| Product code | KYX |
| Recalling firm | Baxter Corporation Englewood |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 8, 2016 |
| FEI number | 1419106 |
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