Device recall
Z-0305-2007: Histochemical PAS (Periodic Acid Schiff) Reaction Set. in vitro diagnostic…
FDA device recall · Class III · EMD Chemicals Inc
Key facts
| Recall number (Z-number) | Z-0305-2007 |
|---|---|
| Recall event | 36096 |
| Product | Histochemical PAS (Periodic Acid Schiff) Reaction Set. in vitro diagnostic. Product size configuration: Set of 4 bottles including Schiff Reagent 225mL, Light Green SF Yellowish Stain 225mL, Sodium Carbonate Solution 225mL, and Periodic Acid Solution 225mL. Each kit provides reagents sufficient for… |
| Product code | KKS |
| Recalling firm | EMD Chemicals Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 6, 2008 |
| FEI number | 2244894 |
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