RecallHawk
Class III Recall

Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plastic tubs; and Tippy Toes brand Sensitivi

PBM Nutritionals, LLC

Summary

The FDA issued a Class III for Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plas by PBM Nutritionals, LLC. Reason: Inadvertent release of rejected product to market.

Details

Source

Food Recall

External ID

F-1493-2023

Action Date

2023-09-13

Status

Terminated

Category

food

Product Description

Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plastic tubs; and Tippy Toes brand Sensitivity Premium Infant Formula, 942g, packaged in composite cans

Lot/Code Info: D05LVJV USE BY 05MAR2025 D06LT7VA USE BY 06MAR2025 UPC Codes: 36800496644 and 681131045513

Quantity Affected: N/A

Reason for Recall

Inadvertent release of rejected product to market

Distribution

IL, AL, IA, GA, MS, IN, AR, CO, FL, VA, OH, WI, PA, NH, AZ, KS, TX, TN, NC, LA, MO, KY, DE, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-16

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.

PBM Nutritionals, LLC has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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

How often does PBM Nutritionals, LLC have FDA actions?

PBM Nutritionals, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1493-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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