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

kate farms Pediatric Peptide 1.5 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 250 mL (8.45…

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.

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

Productkate farms Pediatric Peptide 1.5 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 250 mL (8.45 fl oz) UPC 8 51823-00687 4. 12 count case UPC 00851823006201. Shake Well. A ready-to-use oral and tube feeding formula with enzymatically hydrolyzed organic pea protein. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 93708
Package size250 mL
UPC851823006874

FDA code information

EXPANDED 8-10-2022 Lot Code 0031 / Best By Date 10/27/2022 Lot Code 1031 / Best By Date 10/28/2022 Lot Code 3221 / Best By Date 08/11/2022 Lot Code 3531 / Best By Date 12/19/2022 Lot Code 4221 / Best By Date 08/12/2022 Lot Code 4531 / Best By Date 12/20/2022 Lot Code 6131 / Best By Date 11/12/2022 Lot Code 6721 / Best By Date 10/03/2022 Lot Code 7131 / Best By Date 11/13/2022

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Full FDA record and distribution details

Original product description

kate farms Pediatric Peptide 1.5 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 250 mL (8.45 fl oz) UPC 8 51823-00687 4. 12 count case UPC 00851823006201. Shake Well. A ready-to-use oral and tube feeding formula with enzymatically hydrolyzed organic pea protein. Made for Kate Farms, Inc., 101 Innovation Place, Santa Barbara, CA 93708

Extracted codes and context

TypeCode / valueContext
UPC851823006874 1.5 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 250 mL (8.45 fl oz) UPC 8 51823-00687 4. 12 count case UPC 00851823006201. Shake Well. A ready-to-use oral and tube feeding formula with enzymatically hydro

Original FDA recall reason

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

Recall details

Recall number
F-1672-2022
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-1672-2022

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

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