Device recall
Z-1852-2021: Hydrodissection Cannula (Chang), 27g, labeled as: anodynesurgical, REF 7018…
FDA device recall · Class II · Anodyne Surgical
Key facts
| Recall number (Z-number) | Z-1852-2021 |
|---|---|
| Recall event | 87795 |
| Product | Hydrodissection Cannula (Chang), 27g, labeled as: anodynesurgical, REF 7018 ASICO, REF AS-7638 anodynesurgical, REF 7018NS katena, REF K20-3168 anodynesurgical, REF 104910 MSI, REF CA7800 ACCUTONE, REF AX14784-BULK Walcott Rx Products, REF RX2300NS Walcott Rx Products, REF RX2300 |
| Product code | HMX |
| Recalling firm | Anodyne Surgical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 27, 2022 |
| FEI number | 1929756 |
At a glance
- None 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