Device recall
Z-1977-2021: Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray…
FDA device recall · Class II · Exactech, Inc.
Key facts
| Recall number (Z-number) | Z-1977-2021 |
|---|---|
| Recall event | 87989 |
| Product | Humeral Augmented Tray (HAT) trials that are components of KIT-321HAT. Each tray contains 1 of each of the following catalog numbers for a total of 6 trials/tray: (1) HAT STD Left Tray Trial, Cat. #321-00-01; (2) HAT STD Right Tray Trial, Cat. #321-00-02; (3) HAT LAT Left Tray Trial, Cat… |
| Product code | PHX |
| Recalling firm | Exactech, Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K191561 |
| FEI number | 1038671 |
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