SVS recalls blue nitrile medical gloves due to skin irritation and mislabeling. Affected items have specific size and lot numbers. Consumers should check their product details.
Firm received complaints regarding skin irritation when using the gloves, disintegration of the gloves when used with certain cleaning solutions, and mislabeled products (e.g., outer box indicating one size, but inner box indicating another size).
SVS is recalling blue, nitrile medical gloves that can cause skin irritation and mislabeling. This affects examiners who use gloves to prevent contamination between patients and themselves. The issue means some gloves may not fit correctly or could cause skin problems.
The gloves can cause skin irritation when used, and may disintegrate when exposed to certain cleaning solutions. Mislabeling means some products might have incorrect size information, leading to improper fit.
Examiners and healthcare workers who use these gloves for patient care. Those with sensitive skin or who handle cleaning solutions may be at slightly higher risk due to potential irritation or disintegration.
Check for blue nitrile gloves with beaded cuffs. Look for size labels (XS, S, M, L, XL) and specific lot numbers listed in the product details. The item numbers and UDI codes are also unique to each size.
Review the size, lot number, and UDI code on the product packaging to confirm if it matches the recalled items.
The gloves can cause skin irritation and may disintegrate with certain cleaning solutions, so they are not recommended for use.
Check the product details to see if you have a recalled item. If you do, you should stop using them and contact SVS for further instructions.
Mislabeling means the outer box might indicate one size while the inner box shows another. Check both labels carefully.
We’ve drafted a message you can send SVS to request your refund or repair — edit it as you like.
Subject: Recall Z-2320-2024 — SVS SVS Hello, I own a SVS that is covered by recall Z-2320-2024 from SVS. 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.
