Yakult Nonfat Probiotic Drink; Live and active Lactobacillus casei Shitota; 2.7 FL. OZ. (80…
Recalling firm: Yakult U.S.A. Inc.
Firm testing found trace levels of yeast in the product. Further investigation found the presence of Candida pelliculosa.
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: Sep 20, 2021.
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699235001007FDA code information
Lot code 0601ST03; Best if used by Jul 07 and Jul 08, 2021
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Full FDA record and distribution details
Original product description
Yakult Nonfat Probiotic Drink; Live and active Lactobacillus casei Shitota; 2.7 FL. OZ. (80 mL), 5 individual bottles per pack, 10 packs per case. Bottle UPC: 4520 8812 5 pack UPC: 6 99235 00100 7 Ingredients: Water, Sugar, Nonfat Milk, Glucose, Natural Flavors, Lactobacillus Casei Shirota.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 699235001007 | idual bottles per pack, 10 packs per case. Bottle UPC: 4520 8812 5 pack UPC: 6 99235 00100 7 Ingredients: Water, Sugar, Nonfat Milk, Glucose, Natural Flavors, Lactobacillus Casei Shirota. |
Original FDA recall reason
Firm testing found trace levels of yeast in the product. Further investigation found the presence of Candida pelliculosa.
Recall details
- Recall number
- F-0771-2021
- Event ID
- 88204
- FDA status
- Terminated
- Initiated
- Jun 26, 2021
- Reported
- Jul 14, 2021
- Classified
- Jul 8, 2021
- Terminated
- Sep 20, 2021
- Quantity
- 16,073 cases
- Location
- Fountain Valley, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
CA, MD, VA, WI, NC, NY, GA, FL, WA
Data updated September 16, 2026. View official FDA data ↗
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