Device recall
Z-1133-2026: Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE…
FDA device recall · Class II · MicroPort Orthopedics Inc.
Key facts
| Recall number (Z-number) | Z-1133-2026 |
|---|---|
| Recall event | 98220 |
| Product | Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product Description: HIPTURN FEM HEAD TRIAL 36MM REUSABLE |
| Recalling firm | MicroPort Orthopedics Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3010536692 |
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