Revive MD Ashwagandha Capsules Recalled for Undeclared Milk
NutraCap Labs LLC is recalling Revive MD Ashwagandha Capsules 60ct bottles because the product contains undeclared milk, which poses a risk to consumers with milk allergies.
The agency’s classification
FDA (Food): 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: This recall is classified as FDA Class I by the agency. Although no illnesses or injuries are reported in the source text, the agency's own Class I classification mandates a minimum severity score of 4 per the rubric.
Plain-English summary
NutraCap Labs LLC is recalling Revive MD Ashwagandha Capsules 60ct Bottle (UPC 7 28614 77933 3) due to the presence of undeclared milk in the product. During an FDA investigation, the firm was notified of this allergen mislabeling issue.
Affected lots include LOT #2104054 (expiration date 04/2023) and LOT #2008224 (expiration date 08/2022). Approximately 80,169 various bottles and jars were distributed across the following states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA, and WA.
Consumers who have purchased this product and have a milk allergy or sensitivity should stop using it immediately and dispose of it safely. Those with questions or concerns may contact the recalling manufacturer or their healthcare provider.
The recalled product
- Product
- Revive MD Ashwagandha Capsules 60ct Bottle UPC CODE 7 28614 77933 3
- Manufacturer
- NutraCap Labs LLC
- Affected units
- 80,169
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)
- LOT #2104054 EXP DATE 04/2023 LOT #2008224 EXP DATE 08/2022
Distribution
Part of a larger recall action
This product is one of 106 recalled by NutraCap Labs LLC 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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