Wondfo recalls TCube oral drug test cubes due to risk of foam tip dislodging in mouth, causing choking. Affected models include AMPSO, BARGO, SUPS, BZ030, COC20, MDMAlOO, METSO, OPl40, OXY20, THC2S.
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 could lead to serious injury if the foam tip becomes dislodged during use.
The saliva collection device in the TCube test cubes has a potential to fail, causing the foam tip to become dislodged in the user's mouth. This dislodgement could create a choking hazard, especially if the user is not careful during the test process.
Users of the TCube oral drug test cubes are affected, particularly those who have recently used the product for drug screening. People who test themselves at home or use the device for employment/insurance purposes are most at risk.
Check for the product names AMPSO, BARGO, SUPS, BZ030, COC20, MDMAlOO, METSO, OPl40, OXY20, or THC2S. The product was sold with SKU/Item Number TCUBE-lOBUP and Lot/Batch Number W61080201.
Immediately stop using the TCube One Step Multi-Drug Oral Fluid Test Cube if you have it.
The product has a potential for failure that could cause choking, so it is not safe to use as recalled.
The recall does not specify a remedy, so you should stop using it immediately and contact the manufacturer for further instructions.
The affected models include AMPSO, BARGO, SUPS, BZ030, COC20, MDMAlOO, METSO, OPl40, OXY20, and THC2S.
We’ve drafted a message you can send Wondfo to request your refund or repair — edit it as you like.
Subject: Recall Z-2789-2018 — Wondfo Wondfo Hello, I own a Wondfo that is covered by recall Z-2789-2018 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.
