Device recall
Z-1293-03: CoaguChek brand PT Test Strips; U.S. catalog number 3116247 (professional use)…
FDA device recall · Class I · Roche Diagnostics Corp.
Key facts
| Recall number (Z-number) | Z-1293-03 |
|---|---|
| Recall event | 27193 |
| Product | CoaguChek brand PT Test Strips; U.S. catalog number 3116247 (professional use), 3116239 (patient self test), ex-U.S. catalog numbers 1937642 [packaged 48 strips per box] and 1937634 [packaged 12 strips per box]. |
| Product code | GJS |
| Recalling firm | Roche Diagnostics Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 11, 2004 |
| 510(k) numbers | K962571, K974569 |
| FEI number | 1823260 |
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