Device recall
Z-2103-2017: 16 mm Distraction Pin, Titanium, Qty: 1 per pack; STERILE; Manufactured for…
FDA device recall · Class II · MEDLINE INDUSTRIES INC
Key facts
| Recall number (Z-number) | Z-2103-2017 |
|---|---|
| Recall event | 76298 |
| Product | 16 mm Distraction Pin, Titanium, Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary fixation screw utilized… |
| Product code | LXH |
| Recalling firm | MEDLINE INDUSTRIES INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 9, 2019 |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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