Device recall
Z-1290-2021: Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity…
FDA device recall · Class II · Corin Ltd
Key facts
| Recall number (Z-number) | Z-1290-2021 |
|---|---|
| Recall event | 87293 |
| Product | Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit, titanium alloy shell… |
| Product code | MEH |
| Recalling firm | Corin Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 23, 2022 |
| 510(k) numbers | K130343 |
| FEI number | 3002806725 |
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