Device recall
Z-2779-2020: STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended…
FDA device recall · Class II · HF Acquisition Co. LLC
Key facts
| Recall number (Z-number) | Z-2779-2020 |
|---|---|
| Recall event | 85898 |
| Product | STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives. |
| Product code | LRR |
| Recalling firm | HF Acquisition Co. LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2022 |
| FEI number | 3014534 |
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