FDA Recall United States Terminated Historical recordClass I
Lyons Magnus, Inc
- Product
- PROUCT WAS NOT DISTRIBUTED IN US. The Original Oatly! Oat…
- Published
- September 7, 2022
- Distribution
- Nationwide
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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Sysco Imperial Thickened Dairy Drink. Moderately Thick Honey Consistency. Pasteurized - Made with Grade A 2% Fat Milk, Vitamins A & D. Packaged in the following sized Tetra Pak containers: 1. 8 FL OZ (237 mL) UPC 0 74865-94550 9. Reorder # 0429357. 24 count case UPC 10074865945506. 2. 32 FL OZ (1 QT) 946mL UPC 7 34730-55614 7. Reorder # 4254296. 12 count case UPC 10734730556144. Refrigerate prior to serving. Shake well. Distributed by Sysco Corporation, Houston, Texas 77077. | 10074865945506 | 53,818,025 total units | 1. 8 oz. cartons Lot Code 4212 / Best By Date 11/30/2022; Lot Code 6212 / Best By Date 12/2/2022. EXPANDED 8-10-2022 Lot Code 3102 / Best By Date 08/11/2022. Lot Code 4102 / Best By Date 08/12/2022. Lot Code 7402 / Best By Date 09/14/2022. Lot Code 8402 / Best By Date 09/15/2022. Lot Code 8602 / Best By Date 10/05/2022. Lot Code 9202 / Best By Date 08/27/2022. Lot Code 9602 / Best By Date 10/06/2022. 2. 32 oz. cartons Lot Code 5902 / Best By Date 11/01/2022. Lot Code 6902 / Best By Date 11/02/2022. Lot Code 7212 / Best By Date 12/03/2022. EXPANDED 8-10-2022 Lot Code 0402 / Best By Date 09/07/2022. Lot Code 1702 / Best By Date 10/08/2022. Lot Code 2702 / Best By Date 10/09/2022. |
This recall shares FDA event ID 90667 with 10 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
Responsible company: Lyons Magnus, Inc
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
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A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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