Device recall
Z-0726-2024: PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product…
FDA device recall · Class II · Limacorporate S.p.A
Key facts
| Recall number (Z-number) | Z-0726-2024 |
|---|---|
| Recall event | 93668 |
| Product | PRIMA TT Glenoid Monoblock/Modular reverse TT baseplates: Description/Product Code: BASEPLATE D.25MM REGULAR/1975.14.500, BASEPLATE D.28MM REGULAR/1975.14.800, BASEPLATE D.25MM FULL WEDGED 10-degrees/1975.14.510, BASEPLATE D.28MM FULL WEDGED 10-degrees/1975.14.810, BASEPLATE D.25MM FULL WEDGED… |
| Product code | MBF |
| Recalling firm | Limacorporate S.p.A |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K222427 |
| FEI number | 3008021110 |
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