Cardinal Health recalls PROTEXIS Latex Micro Surgical Gloves Size 7.0 due to potential holes and tears at the folding area around cuffs, which could compromise barrier protection during surgery.
A degradation defect was found that could lead to holes and donning tears at the folding area around the cuffs.
Cardinal Health is recalling PROTEXIS Latex Micro Surgical Gloves Size 7.0 because a defect may cause holes and tears at the cuffs. This could lead to reduced protection from contamination during surgical procedures.
The gloves have a defect that can cause holes and tears at the folding area near the cuffs. This may compromise the barrier protection intended to prevent contamination during surgery.
Operating room personnel who use the recalled gloves for surgical procedures are most at risk. The recall affects specific lot numbers sold between 2019 and 2020.
Check for the lot numbers listed in the recall: TS19060339 through TS20070107. The product is a size 7.0 surgical glove made by Cardinal Health.
Look for the specific lot numbers listed in the recall (TS19060339 through TS20070107) on the glove packaging.
Cardinal Health found a degradation defect that could lead to holes and tears at the folding area around the cuffs, potentially compromising barrier protection during surgery.
The recall does not require immediate action beyond checking the lot numbers. If you have the recalled lot numbers, you should stop using them and contact Cardinal Health for a replacement.
The defect could cause holes and tears at the cuffs, which might reduce protection from contamination during surgery. However, the recall does not indicate an immediate risk of serious injury.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2915-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2915-2020 from Cardinal Health. 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.
