Device recall
Z-0833-04: HENRY SCHEIN(R) 100-3620 Explorer-Single End #23 SE. Barcode *+H658100362003*…
FDA device recall · Class II · Hu-Friedy Mfg Co, Inc.
Key facts
| Recall number (Z-number) | Z-0833-04 |
|---|---|
| Recall event | 28672 |
| Product | HENRY SCHEIN(R) 100-3620 Explorer-Single End #23 SE. Barcode *+H658100362003*. Made in China. For professional use only. Instruments must be cleaned and sterilized prior to use. Distributed by: HENRY SCHEIN, INC. 135 Duryea Road, Melville, NY 11747 USA. This product is a dental explorer made of… |
| Product code | EKB |
| Recalling firm | Hu-Friedy Mfg Co, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 2, 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