Device recall
Z-1588-05: product labeled in part: ''***banicide ADVANCED, A Reusable Sterilizing &…
FDA device recall · Class II · Pascal Co Inc
Key facts
| Recall number (Z-number) | Z-1588-05 |
|---|---|
| Recall event | 32900 |
| Product | product labeled in part: ''***banicide ADVANCED, A Reusable Sterilizing & Disinfecting Solution***Active Ingredient: Glutaraldehyde (1,5 Pentanedial) 3.5%***NET CONTENTS: 3.8l (ONE U.S. GALLON)***Manufactured by Pascal Company, Inc. 2929 N.E. Northup Way P.O. Box 1478 Bellevue, WA 98009-1478… |
| Product code | MED |
| Recalling firm | Pascal Co Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 17, 2011 |
| 510(k) numbers | K012889 |
| FEI number | 3011632 |
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