Dr. Rico Perez Super Kids Colostrum
Recalling firm: FLP LLC
Why it was recalled
Colostrum is declared but label does not declare milk.
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Compare the exact product and package details with the label you have.
ProductDr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.
UPC
879840000446FDA code information
Lot Code 1117002, Expiration Date 04/30/2023. Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025.
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Full FDA record and distribution details
Original product description
Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 879840000446 | supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145. |
| expiration | 04/30/2023 | Lot Code 1117002, Expiration Date 04/30/2023. Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025. |
| expiration | 07/31/2024 | ot Code 1117002, Expiration Date 04/30/2023. Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025. |
| expiration | 11/30/2025 | Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025. |
Original FDA recall reason
Colostrum is declared but label does not declare milk.
Recall details
- Recall number
- F-0822-2023
- Event ID
- 92087
- FDA status
- Ongoing
- Initiated
- Mar 29, 2023
- Reported
- May 17, 2023
- Classified
- May 5, 2023
- Quantity
- Lot 1117002 = 5,760 bottles; Lot 0122003 = 1,800 bottles; Lot 0223539 = 180 bottles
- Location
- Tempe, AZ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Telephone
Where it was distributed
Distributed in CA, FL, NJ, and NY.
FDA source record · F-0822-2023
Data updated September 16, 2026. View official FDA data ↗
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