FDAClass IIIDecember 25, 2019

QuickTox 5 Panel Drug Screen DipCard recall

QuickTox 5 Panel Drug Screen DipCard

Why was QuickTox 5 Panel Drug Screen DipCard recalled?

Mixed Products containing QuickTox 5 Panel Drugs Screen Dipcard (P/N QT11, LOT #188787) and Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX LOT #188744)

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

Catalog Number: QT11 Lot Number: 188787

Product
QuickTox 5 Panel Drug Screen DipCard
Recalling firm
Ameditech Inc
Quantity
3400 units (136 kits)
Distribution
US - AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, and TX. OUS - None
Recall date
December 25, 2019
Classification
Class III
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls