Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1852-2021 — 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

U.S. FDA — Device Enforcement · United States · 2021-04-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1852-2021
Date of alert
2021-04-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Anodyne Surgical
Product category
device
Product type
Devices
Reported risk: The product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.