Cardinal Health recalls PROTEXIS Latex Micro Surgical Gloves Size 8.5 due to potential holes and tears at the folding area. Affected lots include TS19060044 through TS20060005. Consumers should check their lot numbers and contact the manufacturer 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 8.5 because a defect could cause holes and tears at the folding area. This hazard might lead to compromised barrier protection during surgery.
The gloves have a degradation defect that can cause holes and tears at the folding area around the cuffs. This defect may compromise the barrier protection during surgical procedures, potentially leading to contamination exposure.
Operating room personnel who use these gloves for surgical procedures 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 TS19060044 through TS20060005. These gloves were sold between 2019 and 2020 for use in operating rooms.
Look for the lot number on the packaging, which is listed as TS19060044 through TS20060005.
A degradation defect could lead to holes and tears at the folding area around the cuffs, potentially compromising barrier protection during surgery.
Affected lots include TS19060044, TS19060122, TS19060189, TS19080111, TS19080184, TS19080227, TS19090008, TS19090127, TS19100079, TS19100220, TS19110109, TS19110285, TS19110331, TS19120316, TS20050031, TS20050139, TS20050169, TS20050262, TS20060005.
The recall does not require immediate stop use; however, affected lots should be checked and replaced if necessary.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-2918-2020 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-2918-2020 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.
