Wondfo recalls TCube One Step Multi-Drug Oral Fluid Test Cubes due to potential saliva collection device failure causing choking. Users should stop using affected models immediately.
GUANGZHOU WONDFO BIOTECH discovered on the TCube One Step Multi-Drug Oral Fluid Test Cube the potential for failure of the saliva collection device. The use of the saliva collection device could cause the foam tip to become dislodged in the user's mouth creating a choking hazard.
Wondfo is recalling TCube One Step Multi-Drug Oral Fluid Test Cubes because the saliva collection device might dislodge in the user's mouth, creating a choking hazard. This risk affects users who have the specific model numbers listed in the recall.
The saliva collection device in the test cube could become dislodged in the user's mouth during use, leading to a choking hazard. This failure occurs because the foam tip may not stay securely in place, potentially causing the user to choke on the device.
Users of the TCube One Step Multi-Drug Oral Fluid Test Cubes with model numbers AMPSO, BARGO, BZ030, COC20, MDMA100, METSO, MTD30, OPl40, OXY20, THC2S are most at risk. These products were sold with the SKU TCUBE-lOMO and lot number W61080202.
Check for model numbers AMPSO, BARGO, BZ030, COC20, MDMA100, METSO, MTD30, OPl40, OXY20, or THC2S on the product. The product was sold with SKU TCUBE-lOMO and lot number W61080202.
Discontinue use of the TCube One Step Multi-Drug Oral Fluid Test Cubes with the listed model numbers to prevent choking.
The affected model numbers are AMPSO, BARGO, BZ030, COC20, MDMA100, METSO, MTD30, OPl40, OXY20, and THC2S.
Check for model numbers AMPSO, BARGO, BZ030, COC20, MDMA100, METSO, MTD30, OPl40, OXY20, or THC2S on the product. The product was sold with SKU TCUBE-lOMO and lot number W61080202.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Wondfo to request your refund or repair — edit it as you like.
Subject: Recall Z-2788-2018 — Wondfo Wondfo Hello, I own a Wondfo that is covered by recall Z-2788-2018 from Wondfo. 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.
