Device recall
Z-2233-2008: Hamilton Soft Grip Pipettes, 1 ml adjustable volume, model number 55019-40…
FDA device recall · Class II · Hamilton Co
Key facts
| Recall number (Z-number) | Z-2233-2008 |
|---|---|
| Recall event | 48425 |
| Product | Hamilton Soft Grip Pipettes, 1 ml adjustable volume, model number 55019-40 Product is indicated for manual pipetting. |
| Product code | JQW |
| Recalling firm | Hamilton Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 8, 2011 |
| FEI number | 2915796 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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