Saint Charles, MO, United States
Anodyne Surgical recalls
1 recall recorded since 2018, most recently on 21 April 2021. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 21 April 2021
- Terminated
- 27 May 2022
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- 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-BU
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.