Device recall
Z-2798-2020: Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid…
FDA device recall · Class II · Intrinsic Therapeutics, Inc.
Key facts
| Recall number (Z-number) | Z-2798-2020 |
|---|---|
| Recall event | 86121 |
| Product | Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid ACD is indicated for reducing the incidence of reherniation, and reoperation in skeletally mature patients with radiculopathy (with or without back pain) attributed to a posterior or posterolateral herniation, and… |
| Product code | QES |
| Recalling firm | Intrinsic Therapeutics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2020 |
| PMA numbers | P160050 |
| FEI number | 3006232063 |
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