Device recall
Z-1181-2018: Rotating IV Pole Rotating IV Pole falls under the category classified as capital…
FDA device recall · Class II · Ohmeda Medical
Key facts
| Recall number (Z-number) | Z-1181-2018 |
|---|---|
| Recall event | 79452 |
| Product | Rotating IV Pole Rotating IV Pole falls under the category classified as capital equipment, an optional accessory that may be purchased to facilitate attachment and consolidation of patient equipment to one central patient care area. Devices commonly attached to IV poles include IV pumps, feeding… |
| Product code | FOX |
| Recalling firm | Ohmeda Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 17, 2019 |
| FEI number | 1121732 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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