Device recall
Z-2733-2020: Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S…
FDA device recall · Class II · Arthrex, Inc.
Key facts
| Recall number (Z-number) | Z-2733-2020 |
|---|---|
| Recall event | 86021 |
| Product | Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions. |
| Product code | HRS |
| Recalling firm | Arthrex, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 16, 2021 |
| 510(k) numbers | K141478 |
| FEI number | 1220246 |
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