Cardinal Health recalls PROTEXIS Latex Micro Surgical Gloves Size 5.5 due to potential holes and tears at the folding area. Affected lots include TS19060338 through TS20070125. Consumers should check their lot numbers and contact Cardinal Health for details.
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 5.5 because they can develop holes and tears at the folding area around the cuffs. This could lead to contamination during surgery if the gloves are not properly sealed.
The gloves can develop holes and tears at the folding area around the cuffs due to a degradation defect. This defect may compromise the barrier protection during surgical procedures, potentially allowing contamination.
Operating room personnel who use the PROTEXIS Latex Micro Surgical Gloves Size 5.5 are most at risk. The recall affects specific lot numbers produced between 2019 and 2020.
Check the lot number on the packaging, which is listed as TS19060338 through TS20070125. The product is a size 5.5 latex micro surgical glove intended for use in operating rooms.
Look for the lot number on the packaging, which is listed as TS19060338 through TS20070125.
The recall indicates a potential risk of holes and tears at the folding area, so they should not be used until the recall is addressed.
Check the lot number on the packaging. If it matches the affected lots listed, contact Cardinal Health for instructions.
The recall record does not specify a replacement process; contact Cardinal Health directly for details.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2912-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2912-2020 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.
