Sage Products recalls female urine management systems with potential undeclared natural rubber latex adhesive in some lots. Affected units may cause allergic reactions. Contact for return instructions.
A small percentage of devices in three lots of product may contain a tape with a natural rubber latex adhesive which is not declared on the label
Sage Products is recalling certain female urine management systems due to a small percentage of units containing natural rubber latex adhesive that wasn't labeled. This could cause allergic reactions in sensitive individuals.
The product may contain natural rubber latex adhesive that wasn't declared on the label. This could cause allergic reactions in people sensitive to latex. The risk is low as only a small percentage of units are affected.
Women using the Sage PrimaFit External Urine Management System for female anatomy. Those with latex allergies are most at risk.
Check the lot code on the product: 93667, 93614, or 93613. The product is the Sage PrimaFit External Urine Management System for female anatomy with GTIN 00618029600417.
Look for lot codes 93667, 93614, or 93613 on the product label.
The recall is for a small percentage of units that may contain undeclared natural rubber latex adhesive, which could cause allergic reactions in sensitive individuals. The risk is low.
Check the lot code on the product: 93667, 93614, or 93613. The product is the Sage PrimaFit External Urine Management System for female anatomy with GTIN 00618029600417.
The recall does not specify a remedy, so contact Sage Products for further instructions.
We’ve drafted a message you can send Sage Products to request your refund or repair — edit it as you like.
Subject: Recall Z-0356-2024 — Sage Products Sage Products Hello, I own a Sage Products that is covered by recall Z-0356-2024 from Sage Products. 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.
