Device recall
Z-0812-06: MX441B, CVP Manometer. The product is packaged in a cardboard box. The units are…
FDA device recall · Class II · Medex Inc
Key facts
| Recall number (Z-number) | Z-0812-06 |
|---|---|
| Recall event | 35122 |
| Product | MX441B, CVP Manometer. The product is packaged in a cardboard box. The units are packed ten (10) per case. The product is labeled on the outer case with a stick-on label that reads in part, ''**medex Dublin, OH 43016 USA**STERILE***MX441B CVP Manometer**Lot#***Latex Free'' |
| Product code | KRK |
| Recalling firm | Medex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2007 |
| 510(k) numbers | K904674 |
| FEI number | 1526863 |
At a glance
- 1–9 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