Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested
Summary
The FDA issued a Class I for Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supple by IHERB LLC. Reason: Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk..
Details
Source
Food Recall
External ID
F-0846-2021
Action Date
2021-08-18
Status
Terminated
Category
food
Product Description
Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested usage: Simply add 1 scoop (15.38 g) to a 6-8 fl oz. of room temperature water or juice once daily. UPC 8 98220 01828 4 Manufactured for Madre Labs, LLC 301 N. Lake Ave., #600 Pasadena, CA 91101
Lot/Code Info: Finished Product Lot No.: 03011; Expiration Date: 11/2/2023 Item No.: SLM-01828
Quantity Affected: 4508 units
Reason for Recall
Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.
Distribution
Direct sales to customers in AL, AZ, CA, CO, CT, DE, FL, GA, IL, KY, MA, MD, ME, MN, MO, MS,MT, NC, NJ, NM, NV, NY, OH, OR, PA, SC, TN, TX, VA, WA. Foreign customers in UA, UZ, VN, TR, TH, SI, SG, SE, SA, RO, QA, PT, PL, PH, PE, OM, NZ, NO, NL, MY, MX, MO, MD, LV, LU, LT, KZ, KW, KR, KG, JP, JO, IT, IS, IL, IE, ID, JU, HR, HK, GR, GB, FR, ES, EE, DE, GY, NCV, CH, CA, BY, BR, BH, BG, BE, BA, AZ, AU, AO, AM, Al, AE.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-05-24
Company
Pasadena, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (IHERB LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does IHERB LLC have FDA actions?
This is the only FDA action we have on record for IHERB LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0846-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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