F-0761-2019 Class I Terminated

Recalled by Atherstone Foods, Inc. Dba Glass Onion Catering — Richmond, CA

FDA food recall F-0761-2019 was initiated by Atherstone Foods, Inc. Dba Glass Onion Catering on Dec 16, 2018 and is designated Class I. Reason for recall: During internal review is was discovered that the incorrect dressing was used in production of a vegetable wrap that does not declare soy as an ingredient or allergen. The recall status is terminated (terminated Apr 9, 2019). Affected quantity: 114 units.

Recall Details

Product Type
Food
Report Date
Feb 6, 2019
Initiation Date
Dec 16, 2018
Termination Date
Apr 9, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
114 units

Product Description

greens & Grains Hummus & Quinoa Tabouleh Wrap with lemon tahini dressing: Perishable: Keep Refrigerated Plastic container with tamper proof hinged lid Use by 12/19/18 Incorrect dressing was used: Label states: Dressing: Tahini (ground sesame seeds), Lemon Juice, Water, Pomace Olive Oil (refined pomace olive oil, extra virgin Olive Oil), Garlic. Kosher Salt, Black Pepper. Mayonnaise was used in error: Ingredient Statement: Water, Expeller Pressed Canola Oil, Food Starch Modified, Distilled Vinegar, Apple Cider Vinegar, Salt, Soy Protein, Isolate, Xanthan Gum, Lemon Juice Concentrate, Onion Powder, Mixed Tocopherols (Natural Antioxidant), Rosemary Extract, Mustard Oil, Oleores Allergen(s): Soy Manufactured by Glass Onion Catering, Richmond, CA 94804

Reason for Recall

During internal review is was discovered that the incorrect dressing was used in production of a vegetable wrap that does not declare soy as an ingredient or allergen.

Distribution Pattern

Product was distributed to 3 northern CA locations.

Code Information

Use by 12/19/18

Source

Dataset
openFDA food recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for F-0761-2019
openFDA file date
Oct 6, 2026
Loaded by RegDataLab
Oct 6, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.