FDA Recalls Fataway Ultimate Stack Supplement for Unapproved Salicylic Acid
Novacare, LLC is recalling Thin and Slim Fataway Ultimate Stack with Chromium because FDA sampling found unapproved salicylic acid in the dietary supplement.
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 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 agency classified this as an FDA Class I recall, which mandates a severity score of at least 4 per the rubric.
Plain-English summary
Novacare, LLC is recalling Thin and Slim Fataway Ultimate Stack with Chromium, packaged in 120 capsules. The product is distributed by Dale H Enterprises Inc. in Lewisburg, PA, and was sold nationwide under UPC 853002003025.
The recall was initiated because FDA sampling confirmed the presence of salicylic acid in the dietary supplement. The product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA), which is required for drug products.
Consumers who purchased this product should stop using it and contact the distributor or retailer for a refund or further instructions.
The recalled product
- Product
- Thin and Slim Fataway Ultimate Stack with Chromium, packaged per 120 capsules. Distributed by Dale H Enterprises Inc. Lewisburg, PA 17837, www.fataway.org.
- Manufacturer
- Novacare, LLC
- Category
- Drug — Dietary Supplement
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 (1)
- UPC 853002003025
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 13 recalled by Novacare, LLC 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 13 products in this recall →Related recalls
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