Device recall
Z-2762-2019: Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic…
FDA device recall · Class II · Zimmer GmbH
Key facts
| Recall number (Z-number) | Z-2762-2019 |
|---|---|
| Recall event | 83689 |
| Product | Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic implant - Product Usage: The Sidus Stem-Free Shoulder is designed for long-term implantation into the human shoulder joint as a total shoulder arthroplasty in combination with Zimmer or Biomet s glenoid components, or… |
| Product code | PKC |
| Recalling firm | Zimmer GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 20, 2020 |
| 510(k) numbers | K171858 |
| FEI number | 3005233524 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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