Device recall
Z-2714-2017: ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to…
FDA device recall · Class II · Arjo, Inc. dba ArjoHuntleigh
Key facts
| Recall number (Z-number) | Z-2714-2017 |
|---|---|
| Recall event | 77551 |
| Product | ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff. The system is intended… |
| Product code | JOW |
| Recalling firm | Arjo, Inc. dba ArjoHuntleigh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 12, 2022 |
| 510(k) numbers | K143438 |
| FEI number | 1419652 |
At a glance
- 1–9 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