QuickTox 5 Panel Drug Screen DipCard
Reported: December 25, 2019 Initiated: February 15, 2019 #Z-0692-2020
Product Description
QuickTox 5 Panel Drug Screen DipCard
Reason for Recall
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)
Details
- Recalling Firm
- Ameditech Inc
- Units Affected
- 3400 units (136 kits)
- Distribution
- US - AZ, CA, FL, GA, KS, LA, MI, MO, MS, NC, OK, TN, and TX. OUS - None
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
QuickTox 5 Panel Drug Screen DipCard. Recalled by Ameditech Inc. Units affected: 3400 units (136 kits).
Why was this product 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)
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 25, 2019. Severity: Low. Recall number: Z-0692-2020.
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