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FDA source record Class I Terminated

kate farms Peptide 1.5 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00646 1. 12 count case UPC 00851823006379. Shake Well. A ready-to-use or...

Recall Date: 2022-07-22 Recalling Firm: Lyons Magnus, Inc Record Ref: F-1671-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns kate farms Peptide 1.5 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00646 1. 12 count case UPC 00851823006379. Shake Well. A ready-to-use or... and names Lyons Magnus, Inc as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Lyons Magnus, Inc
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2022-07-22
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

kate farms Peptide 1.5 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00646 1. 12 count case UPC 00851823006379. 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

Reason for Recall / Hazard Identified

Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Nationwide

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-1671-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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