Class IIIOngoingVoluntary: Firm initiated
Sato Pharmaceutical Inc.: food recall H-0892-2026
Sato Pharmaceutical Inc. of Torrance, CA recalled Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml… Reason: Product does not meet label claim for Vitamin E. The FDA listed it as Class III in its Enforcement Report dated Jun 10, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co. Ltd.; 30ml container. Packed in single serving, 3 units/pack, and 10 units per pack. Single UPC: 49873-916-11 3pack UPC: 49873-916-15 10pack UPC: 49873-916-07
- Product quantity
- 25,130 units across all package sizes
- Reason for recall
- Product does not meet label claim for Vitamin E.
- Codes, lots and dates on the package
- Lot: Expiration date: single CXW T Jan-27 3pack CXW T Jan-27 10pack PXW Z Mar-26 10pack XXW W Dec-27
- Distribution pattern
- Product was distributed to two domestic consignees who further distribute nationwide.
- Recalling firm
- Sato Pharmaceutical Inc., Torrance, CA
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 12, 2026 |
| Classified by the FDA | Jun 2, 2026 |
| Published in the Enforcement Report | Jun 10, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0892-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.