Device recall
Z-3043-2011: Medtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20…
FDA device recall · Class I · Medtronic, Inc. - Neuromodulation
Key facts
| Recall number (Z-number) | Z-3043-2011 |
|---|---|
| Recall event | 59317 |
| Product | Medtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 ml reservoir size.) Sterilized using ethylene oxide. The pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implantable components of the SynchroMed II Infusion… |
| Product code | LKK |
| Recalling firm | Medtronic, Inc. - Neuromodulation |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 24, 2012 |
| PMA numbers | P860004, P860004S056 |
| FEI number | 2182207 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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