Device recall
Z-1648-2023: Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System…
FDA device recall · Class II · Cytrellis Biosystems, Inc.
Key facts
| Recall number (Z-number) | Z-1648-2023 |
|---|---|
| Recall event | 92187 |
| Product | Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring System System intended for the treatment of moderate and severe wrinkles in the mid and lower face. Model #: Gen 4 |
| Product code | QAI |
| Recalling firm | Cytrellis Biosystems, Inc. |
| Recall class | Class II |
| Status | Completed |
| 510(k) numbers | K202517 |
| FEI number | 3020704367 |
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