Device recall
Z-0336-2012: 10mm x 2.7mm RibLoc Screw, a component of the RibLoc Rib Fracture Plating…
FDA device recall · Class II · Acute Innovations Llc
Key facts
| Recall number (Z-number) | Z-0336-2012 |
|---|---|
| Recall event | 60286 |
| Product | 10mm x 2.7mm RibLoc Screw, a component of the RibLoc Rib Fracture Plating System, Model RBP1202. The product is labeled in parts: "***Ribloc Rib Fracture Plating System***MATERIAL: Titanium***Rx ONLY***NON STERILE***SCREW***ACUTE Innovations LLC 21421 NW Jacobson Road, Suite 700 Hillsboro, OR 97124… |
| Product code | HRS |
| Recalling firm | Acute Innovations Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 6, 2011 |
| 510(k) numbers | K051410 |
| FEI number | 3005670412 |
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