Ansell Healthcare recalls Microflex Diamond Grip Examination Gloves (MF-300) due to potential barrier integrity issues. Affected lots include 2003LG batch 20035314LG. No remedy specified in recall notice.
Examination gloves were shipped inadvertently, without to verify barrier integrity.
Ansell Healthcare is recalling Microflex Diamond Grip Examination Gloves (MF-300) because they were shipped without verifying barrier integrity. This could mean the gloves don't properly prevent contamination during medical exams.
The gloves were shipped without verifying their barrier integrity, which means they might not effectively prevent contamination between patients and examiners. This could lead to improper infection control during medical procedures.
Healthcare workers and medical professionals who use these gloves for patient examinations. Those handling the specific lot 2003LG, batch 20035314LG are most at risk.
Check for the lot number 2003LG and batch number 20035314LG on the packaging. These gloves are used for medical examinations and are disposable.
Look for the lot number 2003LG and batch number 20035314LG on the packaging to identify affected items.
The gloves were shipped without verifying barrier integrity, which could mean they don't effectively prevent contamination during medical exams.
The recall notice does not specify a remedy, so check the product details to see if you have the affected lot and batch numbers.
The recall states that the gloves may not have proper barrier integrity, but no specific safety risks are described in the notice.
We’ve drafted a message you can send Ansell Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0051-2021 — Ansell Healthcare Ansell Healthcare Hello, I own a Ansell Healthcare that is covered by recall Z-0051-2021 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.
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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.
