FDA recall F-2177-2014

Product

Echinacea Agustifolia Root PE 4:1 The product is in powder form extracted from the Echinacea root packed in varying size lined cardboard boxes containing 10 kg or 25 kg.

Reason for recall

Products contain Azoxystrobin for which no tolerance is allowed per 40 CFR 180.507.

Distribution

TN, TX, & WA

Key facts

Status

Terminated

Initiation date

2014-06-09

Report date

2014-07-23

Termination date

2014-11-14

Voluntary/Mandated

Voluntary: Firm initiated

Location

S Hackensack, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-2177-2014