Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix. Net Wt 9oz (255g)…
A. L. Schutzman Company, Inc. recalled this product and the FDA reported the enforcement action on 31 May 2023 as Class II. The recall was initiated by the firm. Label mix-up.

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Culinaria Branded Roasted & Salted Colossal Cashew & Macadamia Mix. Net Wt 9oz (255g) UPC 0 41318-22428 3. Distributed by Schnuck Markets, Inc., St. Louis, MO 63146-6928.
- UPC
- 041318224283
- Reason for recall
- Label mix-up.
- Recalling firm
- A. L. Schutzman Company, Inc.
- Firm location
- Waukesha, Wisconsin, United States
- Classification
- Class II
- Status
- Completed
- Recall number
- F-0952-2023
- Quantity
- 828 cans
- Distribution
- IL, IN, MO
- Initiated
- 26 April 2023
- Reported by FDA
- 31 May 2023
- Firm notified by
- Product codes
- Code is ink jet printed on bottom of can. Lot 3033A9 Best By 2/2/2025
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
- The distribution pattern names 3 states, and the FDA published the enforcement report 5 weeks after the firm began the recall.
- Nuts and seeds carry both hazards at once: they are a major allergen in their own right, and as a low-moisture food they hold Salmonella for months without supporting its growth, which is why a nut butter recall can trace to a lot pressed a year earlier.
Named in the distribution pattern: Illinois, Indiana, Missouri. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Filed under nuts and seeds. A product can sit in more than one.
Other nuts and seeds recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from A. L. Schutzman Company, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2015-12-23 | Honey Mustard Pretzel Mix sold under the following brand and size: Girl Scouts, NET WT 7 oz. (198g). | A. L. Schutzman Company, Inc. | The honey mustard pretzel mix lists whey in the ingredient list but does not list Milk in the Contains statement. | Class I |
| 2015-12-23 | Honey Mustard Mix sold under the following brand: Ashdon Farms, Net Wt. 8 oz. (227 g), UPC 79113-41184 | A. L. Schutzman Company, Inc. | The honey mustard mix lists whey in the ingredient list but does not list Milk in the Contains statement. | Class I |
All 3 records for A. L. Schutzman Company, Inc.
All 2023 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. 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.