RecallHawk
Class II Recall

Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum pe

FLP LLC

Summary

The FDA issued a Class II for Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplemen by FLP LLC. Reason: Colostrum is declared but label does not declare milk..

Details

Source

Food Recall

External ID

F-0822-2023

Action Date

2023-05-17

Status

Ongoing

Category

food

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.

Lot/Code Info: Lot Code 1117002, Expiration Date 04/30/2023. Lot Code 0122003, Expiration Date 07/31/2024. Lot Code 0223539, Expiration Date 11/30/2025.

Quantity Affected: Lot 1117002 = 5,760 bottles; Lot 0122003 = 1,800 bottles; Lot 0223539 = 180 bottles

Reason for Recall

Colostrum is declared but label does not declare milk.

Distribution

Distributed in CA, FL, NJ, and NY.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-29

Company

FLP LLC

Tempe, AZ

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (FLP LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does FLP LLC have FDA actions?

This is the only FDA action we have on record for FLP LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0822-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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