Device recall
Z-1220-2007: IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90…
FDA device recall · Class II · Humagen Fertility Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-1220-2007 |
|---|---|
| Recall event | 38348 |
| Product | IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90 consisting of 30 nylon tube packages of 3 pipettes each. Item # PP-9-90PL. Boxes are labeled in part ***Humagen Fertility Diagnostics, Inc. 2400 Hunter's Way Charlottesville, VA 22911*** |
| Product code | MQK |
| Recalling firm | Humagen Fertility Diagnostics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2007 |
| 510(k) numbers | K000915 |
| FEI number | 1216677 |
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