FDAClass IIAugust 22, 2018

TCube One Step Multi-Drug Oral Fluid Test Cube recall

TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO, BARGO, BZ030,COC20,MDMA100,METSO, MTD30,OPl40,OXY20, THC2S) Product Usage: T-Cube¿ One Step…

Why was TCube One Step Multi-Drug Oral Fluid Test Cube recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

SKU/Item Number, (Lot/Batch Number) TCUBE-lOMO, (W61080202)

Product
TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO, BARGO, BZ030,COC20,MDMA100,METSO, MTD30,OPl40,OXY20, THC2S) Product Usage: T-Cube¿ One Step…
Recalling firm
Guangzhou Wondfo Biotech Co., Ltd.
Quantity
60,000 units
Distribution
US Distribution: in the state of VA.
Recall date
August 22, 2018
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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