Device recall
Z-1089-2024: global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle)…
FDA device recall · Class II · CooperSurgical, Inc.
Key facts
| Recall number (Z-number) | Z-1089-2024 |
|---|---|
| Recall event | 93688 |
| Product | global Medium, Model Numbers LGGG-020 (20mL bottle), LGGG-050 (50mL bottle), LGGG-100 (100mL bottle). Intended use: Culture of human embryos from zygote to blastocyst, embryo transfer. |
| Product code | MQL |
| Recalling firm | CooperSurgical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K142991 |
| FEI number | 1216677 |
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