Device recall
Z-1012-2017: symmetry surgical ULTRA(R) Gravity container, REF numbers: C131310-G, C13134-G…
FDA device recall · Class II · Symmetry Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-1012-2017 |
|---|---|
| Recall event | 75850 |
| Product | symmetry surgical ULTRA(R) Gravity container, REF numbers: C131310-G, C13134-G, C13135-G, C13136-G, C13139-G, C13854-G, C13855-G, C13856-G, C181310-G, C18134-G, C18135-G, C18136-G, C18138-G, C22854-G, C22855-G, C22856-G, C22858-G, C24134-G, C24135-G, C24136-G, C24138, C24138-G Product Usage… |
| Product code | KCT |
| Recalling firm | Symmetry Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 20, 2017 |
| 510(k) numbers | K113776 |
| FEI number | 3007208013 |
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