Device recall
Z-2384-2010: Whatman Body Fluid Collection Paper- 903 California Newborn Screening Card Ref…
FDA device recall · Class II · Whatman, Inc.
Key facts
| Recall number (Z-number) | Z-2384-2010 |
|---|---|
| Recall event | 53819 |
| Product | Whatman Body Fluid Collection Paper- 903 California Newborn Screening Card Ref 110534 903 Card are intended for use by healthcare professionals in the collection and in-vitro storage of neonate human blood. The neonate blood is tested to screen the infant for congenital abnormalities of metabolism… |
| Product code | JKA |
| Recalling firm | Whatman, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 24, 2020 |
| 510(k) numbers | K932661 |
| FEI number | 1281317 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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