# FDA recall Z-1852-2021

> **Anodyne Surgical** · Class II · device recall initiated 2021-04-21.

## 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.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of IL, NJ, TX, MO, CA, PA, WA, and the country of Canada.

## Key facts

- **Recall number:** Z-1852-2021
- **Recalling firm:** Anodyne Surgical
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-04-21
- **Report date:** 2021-06-23
- **Termination date:** 2022-05-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Charles, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1852-2021

## Citation

> AI Analytics. FDA recall Z-1852-2021. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1852-2021. Source: US FDA. Licensed CC0.

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