Device recall
Z-2928-2011: remel Haemophilus Test Medium (Agar), 100mm plates, 10/pk, Ref. #R01503. The…
FDA device recall · Class II · Remel Inc
Key facts
| Recall number (Z-number) | Z-2928-2011 |
|---|---|
| Recall event | 58684 |
| Product | remel Haemophilus Test Medium (Agar), 100mm plates, 10/pk, Ref. #R01503. The firm name on the label is Remel, Lenexa, KS. For use in qualitative procedures by the Clinical and Laboratory Standards Institute (CLSI) as the growth medium for antimicrobial disk diffusion tests with Haemophilus species. |
| Product code | JSO |
| Recalling firm | Remel Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 21, 2013 |
| 510(k) numbers | K892928 |
| FEI number | 1924669 |
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