Device recall
Z-1080-2019: McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers…
FDA device recall · Class III · Cypress Medical Products LLC
Key facts
| Recall number (Z-number) | Z-1080-2019 |
|---|---|
| Recall event | 82312 |
| Product | McKesson Consult Diagnostic Immunochemical Fecal Occult Blood Test, Part numbers 178-CK30T, 178-CT30, 178TBSO, 178-CM25, 178-CK50, 178-CM50, 178-CT50, 178CK30 |
| Product code | KHE |
| Recalling firm | Cypress Medical Products LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 21, 2021 |
| 510(k) numbers | K041202 |
| FEI number | 1451040 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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