Recall archive / FDA food enforcement
Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68... — FDA record F-1602-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 22, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Glucerna original Homemade Vanilla Shake, 8 FL OZ (237 mL). Delicious Snack or Small Meal Replacement. UPC 0 70074-68563 2. Sold in 24 count case, Case UPC 0070074685625. Shake Well. Serve cold. Refrigerate after opening. Manufactured for: Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219. Can be sold in 24 - 8 oz Cartons or individual 8 oz Tetra Pak containers.
- Reason
- Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
- Classification
- Class I
- Recalling firm
- Lyons Magnus, Inc
- Quantity
- 53,818,025 total units
- Agency-reported status
- Terminated
- Source record identifier
- F-1602-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Lot Code 400194X00 / Best By Date 08/01/2023; Lot Code 400204X00 / Best By Date 08/01/2023; Lot Code 400214X00 / Best By Date 08/01/2023; Lot Code 400224X00 / Best By Date 08/01/2023; Lot Code 400234X00 / Best By Date 08/01/2023; Lot Code 410294X00 / Best By Date 09/01/2023; Lot Code 410304X00 / Best By Date 09/01/2023; Lot Code 410314X00 / Best By Date 09/01/2023; Lot Code 410334X00 / Best By Date 09/01/2023; Lot Code 410344X00 / Best By Date 09/01/2023. EXPANDED 08/10/2022 Lot Code 390124X00 / Best By Date 07/01/2023; Lot Code 390134X00 / Best By Date 07/01/2023; Lot Code 390144X00 / Best By Date 07/01/2023. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Nationwide
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Sep 7, 2022
- Recall initiation date
- Jul 22, 2022
- Center classification date
- Aug 30, 2022
- Termination date
- Jul 25, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.