Anodyne Surgical recalls 27g Hydrodissection Cannulas with possible yellowish-brown/greenish-brown residue at the tip. Affected units include specific lot numbers and references from 2010-2011. Contact for remedy details.
The product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula.
Anodyne Surgical is recalling 27g Hydrodissection Cannulas that may have a yellowish-brown or greenish-brown residue at the tip. This residue could cause contamination during medical procedures, making the product unsafe for use.
The cannula may have a yellowish-brown or greenish-brown residue at the tip. This residue could contaminate the surgical site during procedures, potentially leading to infection or other complications.
Medical professionals using the cannulas for procedures like surgery or injections. Those with specific lot numbers or reference codes listed in the recall are most at risk.
Check for the brand name 'Anodyne Surgical' and specific lot numbers or reference codes listed in the recall, such as REF 7018, REF AS-7638, or lot numbers like 201157-08.
Look for the brand name 'Anodyne Surgical' and specific lot numbers or reference codes listed in the recall, such as REF 7018, REF AS-7638, or lot numbers like 201157-08.
The product may have a yellowish-brown or greenish-brown residue at the tip, which could contaminate the surgical site during procedures.
Affected lot numbers include 201157-08, 210071-001, 210071-002, 210143-002, and others as listed in the recall.
The recall does not specify a remedy, so there is no action required beyond checking the product details for affected lot numbers.
We’ve drafted a message you can send Anodyne Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1852-2021 — Anodyne Surgical Anodyne Surgical Hello, I own a Anodyne Surgical that is covered by recall Z-1852-2021 from Anodyne Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
