Device recall
Z-0618-2024: RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The…
FDA device recall · Class II · Acumed LLC
Key facts
| Recall number (Z-number) | Z-0618-2024 |
|---|---|
| Recall event | 93470 |
| Product | RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320, Low Profile Primary Guide is an instrument used with a power system to compress the RibLoc plates onto the bone, determine the length of the screw to install, locate the position of the holes to drill, and provide… |
| Product code | LXH |
| Recalling firm | Acumed LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000125930 |
At a glance
- None 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