Device recall
Z-0817-2007: Medtronic Buffer Solution pH 1.07 500ml REF 9012D1071 Manufactured by/for…
FDA device recall · Class III · Medtronic Neuromodulation
Key facts
| Recall number (Z-number) | Z-0817-2007 |
|---|---|
| Recall event | 37852 |
| Product | Medtronic Buffer Solution pH 1.07 500ml REF 9012D1071 Manufactured by/for Medtronic A/S Tonsbakken 16-18 DK-2740 Skovlunde, Denmark |
| Product code | JCC |
| Recalling firm | Medtronic Neuromodulation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 2, 2008 |
| PMA numbers | DIGITRAPPER-K981733 |
| FEI number | 2182207 |
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