Wondfo recalls T-Cube One Step Multi-Drug Oral Fluid Test Cubes due to risk of foam tip dislodging in mouth, causing choking. Affected units include TCUBE-60 with batch W60680202.
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 T-Cube One Step Multi-Drug Oral Fluid Test Cubes because the saliva collection device might become dislodged in the user's mouth, creating a choking hazard. This could lead to serious injury if the foam tip is accidentally dislodged during use.
The saliva collection device in the T-Cube One Step test cubes can become dislodged in the user's mouth during testing. This dislodged foam tip could cause choking if it moves into the throat or airway.
People who own or use the T-Cube One Step Multi-Drug Oral Fluid Test Cubes with batch number W60680202 are affected. Those performing drug tests at home or for employment/insurance purposes are most at risk.
Check for the product name 'T-Cube One Step Multi-Drug Oral Fluid Test Cube' with batch number W60680202. The product is sold as TCUBE-60 with this specific batch code.
Verify the batch number on the product label to confirm if it matches W60680202.
If you have the affected product, stop using it now to prevent choking risks.
The recalled product has batch number W60680202.
The recall record does not mention any remedy or fix for this product.
Check the product label for batch number W60680202 on the TCUBE-60 model.
We’ve drafted a message you can send Wondfo to request your refund or repair — edit it as you like.
Subject: Recall Z-2787-2018 — Wondfo Wondfo Hello, I own a Wondfo that is covered by recall Z-2787-2018 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.
