PlainRecalls
FDA Devices Moderate Class II Terminated

First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B

Reported: October 7, 2020 Initiated: August 18, 2020 #Z-3047-2020

Product Description

First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B

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.

Details

Recalling Firm
Ameditech Inc
Units Affected
47,005 units
Distribution
US - Nationwide OUS - Australia, France, Germany, New Zealand, Singapore and Spain
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
First Check 14 Panel Drug Cup: (BMC style); AMT Item Number 990700B. Recalled by Ameditech Inc. Units affected: 47,005 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 7, 2020. Severity: Moderate. Recall number: Z-3047-2020.