FDA recall record

IHERB Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and recall — FDA F-0846-2021

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

Class Iclassification
F-0846-2021official record ID
Aug 18, 2021report date

Recall record at a glance

Official recordF-0846-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmIHERB LLC
Report dateAug 18, 2021
Recall initiation dateMay 24, 2021
Quantity4508 units
LocationPasadena, CA, United States

Official 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

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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