Device recall
Z-0069-04: Remel Thayer Martin Agar (Improved), packaged in 10-packs (Cat. #01884)…
FDA device recall · Class II · Remel, Inc
Key facts
| Recall number (Z-number) | Z-0069-04 |
|---|---|
| Recall event | 27473 |
| Product | Remel Thayer Martin Agar (Improved), packaged in 10-packs (Cat. #01884), 15-packs (Cat. #01885), and 100 per case (Cat. #01886). The responsible firm on the label is Remel, Lenexa, KS. |
| Product code | JTY |
| Recalling firm | Remel, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 25, 2004 |
| FEI number | 1924669 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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