Device recall
Z-2303-2008: Histochemical PAS (Periodic Acid Schiff) Reaction Set' Class I, IVD; Set of 4…
FDA device recall · Class III · EMD Chemicals Inc
Key facts
| Recall number (Z-number) | Z-2303-2008 |
|---|---|
| Recall event | 48640 |
| Product | Histochemical PAS (Periodic Acid Schiff) Reaction Set' Class I, IVD; Set of 4 bottles including Schiff Reagent 225 mL, Light Green SF Yellowish Stain 225 mL, Sodium Carbonate Solution 225 mL and Periodic Acid Solution 225 mL' EMD Chemicals, Inc. 480 S. Democrat Road, Gibbstown, NJ 08027 Each kit… |
| Product code | HZT |
| Recalling firm | EMD Chemicals Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 22, 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