Device recall
Z-0990-2012: Flow Tec Nano-Hybrid Flowable Affected Product Syringe Part No. Value Pack Part…
FDA device recall · Class II · Sybron Dental Specialties
Key facts
| Recall number (Z-number) | Z-0990-2012 |
|---|---|
| Recall event | 60693 |
| Product | Flow Tec Nano-Hybrid Flowable Affected Product Syringe Part No. Value Pack Part. No. Shade BEN3784-514 BEN3786-754 A1 BEN3784-532 BEN3786-763 A2 BEN3784-541 BEN3784-738 A3 BEN3784-550 BEN3784-747 A3.5 BEN3784-569 BEN3784-756 A4 BEN3784-578 BEN3784-765 B1 BEN3784-596 BEN3784-774 B2 BEN3784-603… |
| Product code | EBF |
| Recalling firm | Sybron Dental Specialties |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 5, 2012 |
| 510(k) numbers | K052106 |
| FEI number | 2024312 |
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