Cardinal Health recalls Protexis Neoprene surgical gloves size 6.0 with incorrect chemotherapy drug breakthrough times on labels. This could affect operating room use. Contact for details.
Labeling issue in that the breakthrough (i.e., permeation) times for two chemotherapy drugs (Carmustine and Thiotepa) stated on the wallet (primary packaging) of the Protexis Neoprene surgical gloves are incorrect. Additionally, breakthrough times for Mitomycin were added to the same label in error.
Cardinal Health is recalling Protexis Neoprene surgical gloves size 6.0 because the labels incorrectly state when chemotherapy drugs can pass through the gloves. This could lead to improper protection of surgical wounds during procedures.
The gloves have incorrect breakthrough times for chemotherapy drugs like Carmustine and Thiotepa on their labels. This means the gloves might not provide the intended protection for surgical wounds during chemotherapy procedures.
Operating room personnel who use these gloves during surgery may be affected. The risk is low as the issue is a labeling error, not a physical defect.
Check for the product code 2D73DP60 and lot numbers listed in the recall notice. These gloves are light brown, powder-free, and sterile.
Look for the product code 2D73DP60 and lot numbers TS18060125 through TS18090281 on the glove packaging.
The recall is due to incorrect breakthrough times for chemotherapy drugs (Carmustine, Thiotepa, and Mitomycin) listed on the gloves' labels.
No, the recall is for labeling errors, not a physical defect. You can continue using them if you check the label for the correct product code and lot numbers.
Check the product code 2D73DP60 and lot numbers TS18060125 through TS18090281 on the packaging.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0632-2019 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0632-2019 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.
