Pico De Gallo
Reason Potential contamination with Salmonella.
waterfront Bistro Tatar Sauce recall
Recalled by Silver Spring Foods, Inc. · Eau Claire, WI, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Silver Spring is recalling Waterfront Bistro Tartar Sauce because an incorrect back label does not identify egg.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 21130-12242
Quantity: 11092 cases (6 bottles per case)
Food: Sauces, dips & dressings
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.
Best By date of JUL 31 18 S3351 and AUG 28 18 S3351
Where it was sold
Nationwide.
Arkansas Arizona California District of Columbia Delaware Florida Hawaii Iowa Idaho Illinois Indiana Louisiana Massachusetts Maryland Maine Montana North Dakota Nebraska New Hampshire New Mexico Nevada Oregon Rhode Island South Dakota Texas Utah Virginia Vermont Washington Wyoming
FDA's distribution note: Nationwide: AR, AZ, CA, DE, FL, HI, IA, ID,IL, IN, LA, MA, MD, ME, MT, ND, NE, NH, NM, NV, OR, RI, SD, TX, UT, VT, VA, WA, WY, including Washington DC
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Silver Spring Foods, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 22, 2017
- In FDA report of
- Oct 18, 2017
- Terminated
- Jun 27, 2019
- FDA recall number
- F-0019-2018 · event 78176
- Official record
- FDA enforcement report search
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