Device recall
Z-0823-2017: Femoral Integral Shaft & Stem 15x27 HA Coated; Femoral Integral Shaft & Stem…
FDA device recall · Class II · Stanmore Implants Worldwide Ltd.
Key facts
| Recall number (Z-number) | Z-0823-2017 |
|---|---|
| Recall event | 75892 |
| Product | Femoral Integral Shaft & Stem 15x27 HA Coated; Femoral Integral Shaft & Stem 15x30 HA Coated; Femoral Integral Shaft & Stem 30x27 HA Coated; Femoral Integral Shaft & Stem 30x30 HA Coated The product is a component is a systems that is intended for the replacement if diseased or deficient bone around… |
| Product code | KRO |
| Recalling firm | Stanmore Implants Worldwide Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2017 |
| 510(k) numbers | K120992 |
| FEI number | 3004105610 |
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