Device recall
Z-1638-2010: BD Beaver Arthro-Lok Pointed Tip 4mm Blade, REF 376780. Becton Dickinson and…
FDA device recall · Class II · Becton Dickinson and Company
Key facts
| Recall number (Z-number) | Z-1638-2010 |
|---|---|
| Recall event | 52291 |
| Product | BD Beaver Arthro-Lok Pointed Tip 4mm Blade, REF 376780. Becton Dickinson and Company, Waltham, MA 02454. Intended for use in arthroscopic procedures. |
| Product code | HTS |
| Recalling firm | Becton Dickinson and Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 26, 2012 |
| FEI number | 1211998 |
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