CHU MINH TOFU Fried Soybean Cake
Reason All fresh tofu and fried tofu products are recalled because they were made in a facility with no available hot water.
CHU MINH TOFU Fresh Soybean Cake recall
Recalled by Chu Minh Corp · Seattle, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
All fresh tofu and fried tofu products are recalled because they were made in a facility with no available hot water.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
CHU MINH TOFU Fresh Soybean Cake (Tofu), net weight 16 oz. The UPC is 8 18140 00002 2. The product is labeled in parts: "***CHUMINH TOFU***Fresh Soybean Cake (Tofu)***Ingredients: Soybean, Water, Calcium Sulfate***NET WT. 16 OZ***Perishable***Keep Refrigerated***CHUMINH TOFU INCORPORATION***6754 Martin Luther King Way S. Seattle, WA 98118***(206) 723-4273***".
Quantity: unknown
Food: Bread & bakery
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
expiration date: 3/14 and 3/15
Where it was sold
Washington
FDA's distribution note: Products are distributed to one sole consignee in Washington and sold directly to walk-in consumers from the production site.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Chu Minh Corp
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 7, 2013
- In FDA report of
- Apr 10, 2013
- Terminated
- Apr 17, 2013
- FDA recall number
- F-2177-2013 · event 64558
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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