Abbott PediaSure Harvest (Lyons Magnus) – bacterial risk (2022)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Abbott PediaSure Harvest 1.0 Cal, For Tube Feeding. Complete nutrition blend. 8 fl oz (237mL). UPC 0 70074-67963 1. 24 count case UPC 00070074679624. Shake very well. Store unopened at room temperature. Once opened, reclose, refrigerate, and use within 24 hours. Manufactured for Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219-3034.
Brand
Lyons Magnus, Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
EXPANDED 8-10-2022 Lot Code 320184X00 / Best By Date 09/01/2022 Lot Code 330194X00 / Best By Date 10/01/2022 Lot Code 330204X00 / Best By Date 10/01/2022 Lot Code 330204X01 / Best By Date 10/01/2022 Lot Code 330214X00 / Best By Date 10/01/2022 Lot Code 350264X00 / Best By Date 12/01/2022 Lot Code 360274X00 / Best By Date 01/01/2023 Lot Code 360284X00 / Best By Date 01/01/2023 Lot Code 370014X00 / Best By Date 02/01/2023 Lot Code 370024X00 / Best By Date 02/01/2023 Lot Code 380034X00 / Best By Date 03/01/2023 Lot Code 380044X00 / Best By Date 03/01/2023 Lot Code 380054X00 / Best By Date 03/01/2023 Lot Code 380064X00 / Best By Date 03/01/2023 Lot Code 380074X00 / Best By Date 03/01/2023 Lot Code 380074X01 / Best By Date 03/01/2023 Lot Code 390084X00 / Best By Date 04/01/2023 Lot Code 390094X00 / Best By Date 04/01/2023
Lyons Magnus, Inc is recalling Abbott PediaSure Harvest 1.0 Cal, For Tube Feeding. Complete nutrition blend. 8 fl oz (237mL). UP due to Findings and potential for Cronobacter sakazakii and Clostridium botulinum.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026