Device recall
Z-0532-2012: Super Valu (Appraise) Combo Kit, Product A1773, each kit packed in a bag or…
FDA device recall · Class II · Heritage Labs International LLC
Key facts
| Recall number (Z-number) | Z-0532-2012 |
|---|---|
| Recall event | 57863 |
| Product | Super Valu (Appraise) Combo Kit, Product A1773, each kit packed in a bag or envelope. (This kit has since changed to product A8302, which will be listed separately due to the new part number.) Each kit contains 1 Triad Medium Alcohol Prep Pad, Cat. No. 10-3001, NDC 50730-3001-0, blood specimen… |
| Product code | LCP |
| Recalling firm | Heritage Labs International LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 26, 2012 |
| 510(k) numbers | K990899 |
| FEI number | 1000118383 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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