Device recall
Z-0526-05: Dental Explorer #2 D/E, Mfr. Part Code/Product Code 101-0913, distributed under…
FDA device recall · Class II · Hu-Friedy Mfg Co, Inc.
Key facts
| Recall number (Z-number) | Z-0526-05 |
|---|---|
| Recall event | 30882 |
| Product | Dental Explorer #2 D/E, Mfr. Part Code/Product Code 101-0913, distributed under the Henry Schein label. Classification Name: 21CFR 872.4565; 510(k) exempt, Class I device, Device Listing # B057701. Product is labeled in part, HENRY SCHEIN 101-0913 Explorer #2 D/E. +H658101091306. Made in China. For… |
| Product code | EKB |
| Recalling firm | Hu-Friedy Mfg Co, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 24, 2012 |
| FEI number | 1416605 |
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