GnuPharma Stress 100% Herbal Supplement 60 Capsules

GnuPharma Corp. recalled GnuPharma Stress 100% Herbal Supplement 60 Capsules in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on May 8, 2017.

The recall was triggered by possible E. coli contamination: "1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)" Shiga toxin-producing E. coli can cause severe cramps and bloody diarrhea, and in serious cases can lead to kidney damage.

Distribution was limited; the FDA record lists "US." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Owasso, OK. The recall covers 131 bottles of product. The FDA has Terminated this recall (first reported Jul 26, 2017), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.