Unomedical recalls VariSoft Infusion Sets with incorrect "Trusteel" packaging. Affected units may have packaging errors that could lead to improper use. Contact for return instructions.
Specific VariSoftTM Infusion Sets were packaged using incorrect secondary packaging (boxes) branded "Trusteel Infusion Set".
Unomedical is recalling specific VariSoft Infusion Sets that were packaged with incorrect secondary boxes labeled "Trusteel Infusion Set". This packaging error could lead to users receiving the wrong product, potentially causing improper use.
The sets were packaged with boxes branded "Trusteel Infusion Set" instead of the correct branding. This could lead to users receiving the wrong product, which might cause improper use during medical treatments.
Healthcare professionals and patients using the recalled VariSoft Infusion Sets for medical treatments. Those who received the sets with "Trusteel" packaging on the box are most at risk.
Check for boxes labeled "Trusteel Infusion Set" on the secondary packaging. The product code is 1726035 and lot number 6005241. The UDI-DI is 05705244018747.
Look for boxes labeled "Trusteel Infusion Set" on the secondary packaging.
The product code is 1726035.
Lot number 6005241.
Check for boxes labeled "Trusteel Infusion Set" on the secondary packaging. The product code is 1726035 and lot number 6005241.
We’ve drafted a message you can send Unomedical to request your refund or repair — edit it as you like.
Subject: Recall Z-3186-2024 — Unomedical Unomedical Hello, I own a Unomedical that is covered by recall Z-3186-2024 from Unomedical. 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.
