Device recall
Z-2677-2011: Remel Spectra MRSA, Ref R01821, 10 plates per package, and Ref R01822, 100…
FDA device recall · Class II · Remel Inc
Key facts
| Recall number (Z-number) | Z-2677-2011 |
|---|---|
| Recall event | 59005 |
| Product | Remel Spectra MRSA, Ref R01821, 10 plates per package, and Ref R01822, 100 plates per package. The firm name on the label is Remel, Lenexa, KS. The product is a selective and differential chromogenic medium recommended for use in the qualitative detection of nasal colonization of… |
| Product code | JSO |
| Recalling firm | Remel Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 18, 2013 |
| 510(k) numbers | K092407 |
| 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