Ansell Healthcare recalls PI Green surgical gloves (ref 20685255-20685290) because some sterile pouches weren't completely sealed, risking contamination during use.
Some surgical glove sterile pouches were not completely sealed.
Ansell Healthcare is recalling PI Green surgical gloves with specific reference numbers because some sterile pouches weren't fully sealed. This could lead to contamination of the gloves during medical procedures, posing a risk to patient safety.
The sterile pouches for the gloves weren't completely sealed, which could allow contaminants to enter the gloves during storage. This might compromise the sterility of the gloves when used in medical procedures.
Healthcare professionals and medical facilities using the recalled PI Green surgical gloves. Those most at risk are individuals performing surgeries where sterile gloves are critical.
Check for the reference numbers 20685255 through 20685290 on the product packaging. The lot numbers listed in the recall include 2203434204 and specific UDI-DI codes.
Verify the reference numbers on the packaging to confirm if your gloves are in the recalled range (20685255-20685290).
The recall is happening because some sterile pouches for the gloves weren't completely sealed, which could lead to contamination during use.
Check the reference numbers on the packaging; recalled gloves have reference numbers from 20685255 through 20685290.
The recall record does not specify a remedy, so no action is required beyond checking if your gloves are in the recalled range.
We’ve drafted a message you can send Ansell Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0096-2024 — Ansell Healthcare Ansell Healthcare Hello, I own a Ansell Healthcare that is covered by recall Z-0096-2024 from Ansell Healthcare. 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.