Cardinal Health recalls PROTEXIS Latex Micro Surgical Gloves Size 8.0 due to potential holes at cuffs causing contamination risks during surgery. Affected lots listed in the recall notice.
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 8.0 because they can develop holes at the cuff area, which might lead to contamination during surgical procedures. This is a serious issue for operating room staff who rely on these gloves for protection.
The gloves can develop holes at the folding area around the cuffs due to a degradation defect. This could allow contaminants to enter during surgical procedures, increasing the risk of infection or contamination.
Operating room personnel using these gloves for surgery are most at risk. The recall affects specific lots of gloves sold to hospitals and surgical facilities.
Check for the product name 'PROTEXIS Latex Micro Surgical Gloves Size 8.0' and lot numbers listed in the recall notice, such as TS19060095 through TS20060084.
Inspect the gloves for holes or tears at the folding area around the cuffs before use.
The recall states these gloves can develop holes at the cuffs, which could lead to contamination during surgery. They are not safe for use until the issue is addressed.
The recall does not specify a remedy, so you should check for holes at the cuffs and avoid using them if you find damage.
Affected lots include TS19060095 through TS20060084 as listed in the recall notice.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2917-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2917-2020 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.
