Food, drugs, devices › Giant Eagle, Inc.
Food recall: Market District Wasabi Soybeans; Net Wt. 6 OZ.; Best By 3/6/17
FDA enforcement event 76186 is a food recall by Giant Eagle, Inc. of Pittsburgh, PA, initiated 29 Sep 2016 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 43% of the 799 food enforcement events initiated in 2016 carry the same class.
Status: Terminated, terminated 6 Mar 2017. Initiation: voluntary: firm initiated. Giant Eagle, Inc. has 31 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Giant Eagle, Inc., Pittsburgh, PA.
Reason for recall
"Undeclared Wheat and Soy Allergen. Packages contained wasabi soybeans. The top label on the lid stated Wasabi Soybeans, however the ingredient label on the bottom of the container was for Wasabi Peas which does not include Wheat and Soy allergens ingredients."
Distribution
"OH, PA, WV"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1467-2017 | Market District Wasabi Soybeans; Net Wt. 6 OZ.; Best By 3/6/17 | 432 units | Class II | Terminated | 15 Feb 2017 |
Context
Other enforcement events for Giant Eagle, Inc.
All 31 events for Giant Eagle, Inc.
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Undeclared Wheat and Soy Allergen. Packages contained wasabi soybeans. The top label on the lid stated Wasabi Soybeans, however the ingredient label on the bottom of the container was for Wasabi Peas which does not include Wheat and Soy allergens ingredients."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "OH, PA, WV"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 6 Mar 2017. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.