Device recall
Z-0852-2016: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF is an interbody device…
FDA device recall · Class II · Stryker Spine
Key facts
| Recall number (Z-number) | Z-0852-2016 |
|---|---|
| Recall event | 73179 |
| Product | AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF is an interbody device system that uses hydraulic pressure to expand the implant in-situ. The purpose of the AccuLIF PL Tubing Set (cat#900301) and AccuLIF TL Tubing Set (cat#905103) is to deliver pressurized saline from a syringe to the… |
| Product code | MAX |
| Recalling firm | Stryker Spine |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2016 |
| 510(k) numbers | K143616 |
| FEI number | 3004024955 |
At a glance
- 1–9 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