Device recall
Z-1331-2012: Surgipath Cyto Jar Fixative; a 120 mL clear, leakproof container prefilled with…
FDA device recall · Class III · Leica Biosystems Richmond Inc.
Key facts
| Recall number (Z-number) | Z-1331-2012 |
|---|---|
| Recall event | 61276 |
| Product | Surgipath Cyto Jar Fixative; a 120 mL clear, leakproof container prefilled with 45 mL of preservative containing polyethylene glycol for the convenient collection, fixation and preservation of all cytologic specimens, 50 jars per case; for in vitro diagnostic use only; Leica Biosystems, 5205 Rt. 12… |
| Product code | LEA |
| Recalling firm | Leica Biosystems Richmond Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 20, 2012 |
| FEI number | 1419341 |
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