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.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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.
- Category
- Food — Dietary Supplement
- 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.
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