Z-3048-2020 Class II Terminated
FDA device recall Z-3048-2020 was initiated by Ameditech Inc on August 18, 2020 and is designated Class II. Reason for recall: Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling. The recall status is terminated (terminated September 30, 2024). Affected quantity: 41,340 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 7, 2020
- Initiation Date
- August 18, 2020
- Termination Date
- September 30, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 41,340 units
Product Description
First Check 2 Panel Drug Cup: (THC/COC); AMT Item Number 990600B
Reason for Recall
Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.
Distribution Pattern
US - Nationwide OUS - Australia, France, Germany, New Zealand, Singapore and Spain
Code Information
ALL Lots Within Expiry