Device recall
Z-2417-2012: Verify Bowie-Dick Test Card, Model #S3098, Steris Biological Operations, 9325…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-2417-2012 |
|---|---|
| Recall event | 63129 |
| Product | Verify Bowie-Dick Test Card, Model #S3098, Steris Biological Operations, 9325 Pinecone Drive, Mentor, OH 44060 The Verify Bowie-Dick Test Card consists of a card printed on one side with bars of chemical indicator ink. On the opposite side of the card, space is provided for critical cycle… |
| Product code | MLR |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 27, 2013 |
| 510(k) numbers | K897045 |
| FEI number | 1527821 |
At a glance
- 1–9 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