Device recall
Z-1690-2013: MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery…
FDA device recall · Class I · Codman & Shurtleff, Inc.
Key facts
| Recall number (Z-number) | Z-1690-2013 |
|---|---|
| Recall event | 65420 |
| Product | MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-4200 (20ml pump) US 91-4200. Intended for the intrathecal delivery of Baclofen or Morphine. |
| Product code | LKK |
| Recalling firm | Codman & Shurtleff, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 21, 2015 |
| PMA numbers | P890055 |
| FEI number | 3002947440 |
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