Device recall
Z-0165-04: AEROSET Immunoglobulin M, list number 1E01-01, manufactured by Abbott…
FDA device recall · Class II · Abbott Laboratories Diagnostic Div
Key facts
| Recall number (Z-number) | Z-0165-04 |
|---|---|
| Recall event | 27178 |
| Product | AEROSET Immunoglobulin M, list number 1E01-01, manufactured by Abbott Laboratories, South Pasadena, CA |
| Product code | DFT |
| Recalling firm | Abbott Laboratories Diagnostic Div |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 26, 2003 |
| 510(k) numbers | K982132 |
| FEI number | 2018433 |
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