Cardinal Health recalls PROTEXIS Latex Micro Surgical Gloves Size 6.0 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 6.0 because a defect may cause holes and tears at the cuffs. This could lead to contamination during surgical procedures if the gloves are used improperly.
The gloves may develop holes and tears at the folding area around the cuffs due to a degradation defect. This could compromise the barrier protection function during surgery, potentially allowing contamination to reach the surgical site.
Operating room personnel who use these 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: TS19060043 through TS20070183. These gloves are sold as disposable surgical gloves for operating room use.
Look for the lot numbers listed in the recall: TS19060043 through TS20070183 on the packaging.
If you have the recalled lot numbers, stop using these gloves immediately as they may tear at the cuffs.
The recall is due to a degradation defect that could cause holes and tears at the folding area around the cuffs, potentially compromising barrier protection during surgery.
If you have the recalled lot numbers, stop using them immediately and contact Cardinal Health for further instructions.
The gloves may have a defect that could cause holes and tears at the cuffs, so they should not be used if they are from the recalled lot numbers.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2913-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2913-2020 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.
