Device recall
Z-1219-2024: LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell…
FDA device recall · Class II · Waldemar Link GmbH & Co. KG (Mfg Site)
Key facts
| Recall number (Z-number) | Z-1219-2024 |
|---|---|
| Recall event | 93944 |
| Product | LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12 |
| Product code | LZO |
| Recalling firm | Waldemar Link GmbH & Co. KG (Mfg Site) |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K190535 |
| FEI number | 3003386935 |
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