IHERB LLC Recall: Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.
United States
TerminatedClass I
- Company
- IHERB LLC
- Product
- Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Gi…
- Recall date
- May 24, 2021
- Terminated
- September 1, 2021
- Source
- FDA
Reason for recall
Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 4508 units | Finished Product Lot No.: 03011; Expiration Date: 11/2/2023 Item No.: SLM-01828 |
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.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0846-2021
- Event ID
- 88007
- Status
- Terminated
- Classification
- Class I
- Company
- IHERB LLC
- 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
- Quantity
- 4508 units
- Reason
- Informed by contract manufacturer that the MCT ingredient used in their product was under recall due to undeclared milk.
- Recall initiation date
- May 24, 2021
- Report date
- August 18, 2021
- Classification date
- Not published in this source record
- Termination date
- September 1, 2021
- Distribution pattern
- 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.
- UPC, lot, and code information
- Finished Product Lot No.: 03011; Expiration Date: 11/2/2023 Item No.: SLM-01828
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: IHERB LLC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alabama | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| Maine | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| Montana | 1 |
| North Carolina | 1 |
| New Jersey | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Virginia | 1 |
| Washington | 1 |
| Idaho | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
