Device recall
Z-0081-2012: Medpro AccuFlo Elastomeric Infusion Device, Model #CT-0020-270C, packaged…
FDA device recall · Class I · Progressive Medical Inc
Key facts
| Recall number (Z-number) | Z-0081-2012 |
|---|---|
| Recall event | 59981 |
| Product | Medpro AccuFlo Elastomeric Infusion Device, Model #CT-0020-270C, packaged 12/box. The box label shows the product is Manufactured By: Medpro International (Thailand) Ltd. for Medpro Corporation Pte. Ltd., Singapore. The devices are intended for patients requiring intravenous, percutaneous… |
| Product code | MEB |
| Recalling firm | Progressive Medical Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 19, 2011 |
| 510(k) numbers | K081905 |
| FEI number | 3000236238 |
At a glance
- 1–9 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