Aldi Inc FDA recall records
The FDA has published 7 food recall enforcement records naming Aldi Inc between 2012 and 2020, covering 5 separate recall events. The firm is recorded in Illinois. Data last updated 2 September 2026.
- Records of 29,386
- 7
- Share of all recalls
- 0%
- Class I of 7
- 1
- Reported between
- 2012 to 2020
What these records are
Every record on this page was published by the FDA in the openFDA food enforcement database. 7 records cover 5 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.
1 of these records are Class I, 5 Class II and 1 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.
What was recalled for
A single record can name more than one hazard, so these counts overlap.
By year
Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.
Where the recalling firms are
The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.
Most recently reported
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2020-05-13 | Simply Nature Organic Red Split Lentils, 16 oz bag, UPC 041498299507 | Aldi Inc | Product may contain undeclared wheat | Class II |
| 2020-05-13 | Simply Nature Organic Green Lentils, 16 oz bag, UPC 041498299514 | Aldi Inc | Product may contain undeclared wheat | Class II |
| 2018-11-14 | Millville Maple & Brown Sugar Instant Oatmeal 15.1 oz. 10 individual serving size packets per 15.1oz retail unit. UPC: 041498 149628 | Aldi Inc | Complaints of insects in product | Class II |
| 2018-08-15 | AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits | Aldi Inc | ALDI has voluntarily recalled AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits and Limu Ahi Poke Hawaiian Poke Kits due to storing the products at temperatures above freezing prior to consumption which can render the products unsafe for consumption. | Class II |
| 2018-08-15 | AnnaSea Limu Ahi Poke Hawaiian Poke Kits | Aldi Inc | ALDI has voluntarily recalled AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits and Limu Ahi Poke Hawaiian Poke Kits due to storing the products at temperatures above freezing prior to consumption which can render the products unsafe for consumption. | Class II |
| 2017-12-27 | Choceur Dark Chocolate Bars, 5.29 oz., 20 units/case | Aldi Inc | ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the potential presence of almond pieces, which are an undeclared treenut allergen. | Class I |
| 2012-07-11 | Northern Catch Harvest of the Sea Fancy Whole Oysters and SeaNet Fancy Whole Oysters; Net Wt. 8 oz (227g) cans, 12 cans per carton; Distributed by Aldi Inc., Batavia, IL 60510-1477; Product of Korea; UPC 0 41498 11984 3 | Aldi Inc | The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health. | Class III |
Questions
- How many FDA recalls has Aldi Inc had?
- The FDA has published 7 food recall enforcement records naming Aldi Inc between 2012 and 2020. Those records cover 5 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
- Does a high recall count mean a firm is unsafe?
- Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.
A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.