Check the Batch
Class ITerminated in FDA datasetRecall initiated Jul 22, 2022

Sweetie Pie Organics Lactation Smoothie Apple Pear. 11.1 FL OZ (330 mL)

Recalling firm: Lyons Magnus, Inc

Why it was recalled

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 25, 2024.

Check your package

Compare the exact product and package details with the label you have.

ProductSweetie Pie Organics Lactation Smoothie Apple Pear. 11.1 FL OZ (330 mL) UPC 8 56334-00254 4. No. 975001. Packaged in the following configurations: 1. 12 count case 2. 4 count wrap UPC 856334002575. Refrigerate after opening and consume within 24 hours. Distributed by HandiCraft Company St. Louis, MO 63116
Package size11.1 FL OZ
UPC856334002544, 856334002575

FDA code information

Lot Code 5512 / Best By Date 06/03/2024; Lot Code 6512 / Best By Date 06/04/2024; Lot Code 7512 / Best By Date 06/05/2024. EXPANDED 8-10-2022 Lot Code 4921 / Best By Date 10/21/2023 Lot Code 9021 / Best By Date 07/28/2023

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Sweetie Pie Organics Lactation Smoothie Apple Pear. 11.1 FL OZ (330 mL) UPC 8 56334-00254 4. No. 975001. Packaged in the following configurations: 1. 12 count case 2. 4 count wrap UPC 856334002575. Refrigerate after opening and consume within 24 hours. Distributed by HandiCraft Company St. Louis, MO 63116

Extracted codes and context

TypeCode / valueContext
UPC856334002544weetie Pie Organics Lactation Smoothie Apple Pear. 11.1 FL OZ (330 mL) UPC 8 56334-00254 4. No. 975001. Packaged in the following configurations: 1. 12 count case 2. 4 count wrap UPC 856334002575.
UPC856334002575ged in the following configurations: 1. 12 count case 2. 4 count wrap UPC 856334002575. Refrigerate after opening and consume within 24 hours. Distributed by HandiCraft Company St. Louis, MO 63116

Original FDA recall reason

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Recall details

Recall number
F-1636-2022
Event ID
90667
FDA status
Terminated
Initiated
Jul 22, 2022
Reported
Sep 7, 2022
Classified
Aug 30, 2022
Terminated
Jul 25, 2024
Quantity
53,818,025 total units
Location
Fresno, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

Nationwide

FDA source record · F-1636-2022

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.