The Recall Desk
SevereFDA (Food)·F-0297-2017·Announced 2017-07-26

GnuPharma Relief Herbal Supplement Recalled for Failed Testing

GnuPharma Corp. is recalling GnuPharma Relief 100% Herbal Supplement because one ingredient failed identity testing and two failed microbiological testing for E. coli.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall involves E. coli contamination, which is a high-risk pathogen, and the FDA has classified the recall as Class II, meeting the criteria for a Severe severity score.

Plain-English summary

GnuPharma Corp. is recalling 244 bottles of GnuPharma Relief 100% Herbal Supplement, 60 capsules. The recall covers products manufactured prior to May 8, 2017, which were distributed in the United States.

The recall was initiated because one ingredient failed identity testing and two ingredients failed microbiological testing for E. coli. The FDA has classified this recall as Class II.

Consumers who have this product should stop using it and contact GnuPharma Corp. for further instructions.

The recalled product

Product
GnuPharma Relief 100% Herbal Supplement 60 Capsules
Manufacturer
GnuPharma Corp.
Affected units
244

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • products manufactured prior to May 8th
  • 2017.

Distribution

Distribution scope not specified by the agency.

Part of a larger recall action

This product is one of 6 recalled by GnuPharma Corp. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 6 products in this recall →