Wishgarden Herbs Recalls Happy Ducts Compress Due to Microbial Contamination
Wishgarden Herbs is recalling 46 jars of Happy Ducts Compress because the product tested positive for Cronobacter Sakazakii.
The agency’s classification
FDA (Drugs): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
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 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of 5 according to the rubric.
Plain-English summary
Wishgarden Herbs, Incorporated is recalling 46 jars of Happy Ducts Compress, a 3 oz. plastic jar product. The recall is due to microbial contamination, as the product tested positive for Cronobacter Sakazakii.
The affected product is identified by Lot # 53664 and an expiration date of 08/2022. It was distributed nationwide in the USA, as well as in Egypt and Canada.
Consumers should stop using the product and contact the recalling firm for further instructions.
The recalled product
- Product
- Happy Ducts Compress, 3 oz. plastic jar, www.wishgardenherbs.com, Boulder, CO. 80301. UPC 6 56490 20223 5
- Manufacturer
- Wishgarden Herbs, Incorporated
- Category
- Drug — Herbal Supplement
- Affected units
- 46
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)
- Lot # 53664
- Exp 08/2022
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Wishgarden Herbs, Incorporated under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 3 products in this recall →Related recalls
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- SevereRecall of Cord Care Powder Due to Cronobacter Sakazakii Contamination
FDA (Drugs) · 2021-01-06
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