Hydrodissection Cannula — Class II medical device recall Z-1852-2021
Terminated recall by Anodyne Surgical, reported 2021-06-23, distributed nationwide. The product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula.
| Recall number | Z-1852-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Anodyne Surgical, Saint Charles, MO, United States |
| Recall initiated | 2021-04-21 |
| Classified | 2021-06-11 |
| Reported by FDA | 2021-06-23 |
| Terminated | 2022-05-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 8,452 units |
| Lot numbers | 200359-003, 200580-006, 2010006-02, 201067-003, 201068-020, 201108-005, 201108-017, 201108-018, 201144-002, 201154-007, 201157-08, 210039-002, 210070-0001, 210071-001, 210071-002, 210080-01, 210127-001, 210142-002, 210143-002 |
| Model numbers | 104910, 104910MSI, 7018, 7018NS, AS-7638, AX14784-BULK, CA7800, K20-3168, RX2300, RX2300NS |
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
Reason for recall
The product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1852-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.