Device recall
Z-1550-2009: Medtronic One Source Pack, Catalog Numbers: ATLS21, ATLS24, ATLS2469, EC1S24…
FDA device recall · Class II · Medtronic Cardiovascular Revascularization & Surgical Therap
Key facts
| Recall number (Z-number) | Z-1550-2009 |
|---|---|
| Recall event | 51785 |
| Product | Medtronic One Source Pack, Catalog Numbers: ATLS21, ATLS24, ATLS2469, EC1S24, EC2S00, EC2S24, EE1S048 and EE2S21. Kits are packaging convenience kits containing previously released sterile-pack products and accessories. |
| Product code | OEU |
| Recalling firm | Medtronic Cardiovascular Revascularization & Surgical Therap |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 22, 2012 |
| FEI number | 1000116158 |
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