Class ITerminated in FDA datasetRecall initiated May 24, 2021

Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt.…

Recalling firm: IHERB LLC

Why it was recalled

Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 1, 2021.

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ProductSolumeve 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
Package size14.1 oz
UPC898220018284

FDA code information

Finished Product Lot No.: 03011; Expiration Date: 11/2/2023 Item No.: SLM-01828

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Full FDA record and distribution details

Original 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

Extracted codes and context

TypeCode / valueContext
UPC898220018284p (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
expiration11/2/2023Finished Product Lot No.: 03011; Expiration Date: 11/2/2023 Item No.: SLM-01828
lot03011Finished Product Lot No.: 03011; Expiration Date: 11/2/2023 Item No.: SLM-01828

Original FDA recall reason

Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.

Recall details

Recall number
F-0846-2021
Event ID
88007
FDA status
Terminated
Initiated
May 24, 2021
Reported
Aug 18, 2021
Classified
Aug 6, 2021
Terminated
Sep 1, 2021
Quantity
4508 units
Location
Pasadena, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

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.

FDA source record · F-0846-2021

Data updated September 16, 2026. View official FDA data ↗

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