Zinger Pickle products under the following labels: 1. Gedney Zinger Chips, item 18800…
Gedney Foods Product, LLC recalled this product and the FDA reported the enforcement action on 30 July 2025 as Class II. The recall was initiated by the firm. Products were slated for disposal due to product and container damage, but were inadvertently sold.

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
- Zinger Pickle products under the following labels: 1. Gedney Zinger Chips, item 18800, 24 fl oz. (1-1/2 Pt) 710mL. UPC 0 41660-00188 4. 2. Gedney Zingers Dill Babies, item 18600, Net 24 fl oz. (1-1/2 Pts) 710mL. UPC 0 41660-00186 0. Refrigerate after opening. Distributed by Gedney Foods Co, Burnsville, MN 55438 Product of Mexico.
- UPC
- 041660001884
- Reason for recall
- Products were slated for disposal due to product and container damage, but were inadvertently sold.
- Recalling firm
- Gedney Foods Product, LLC
- Firm location
- Bloomington, Minnesota, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- H-0329-2025
- Quantity
- 3520 cases total 12 jars per case
- Distribution
- MN
- Initiated
- 9 June 2025
- Reported by FDA
- 30 July 2025
- Terminated
- 14 August 2025
- Firm notified by
- Letter
- Product codes
- 1. Lot Code: 4218 2. Lot Code: 4269
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 is one of 3 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 3 separate recalls, which almost every published figure does, overstates it by a factor of 3. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 3 of them.
- The recall ran for 2 months, from 9 June 2025 to termination on 14 August 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 1 state, and the FDA published the enforcement report 7 weeks after the firm began the recall.
- Recalls of a snack or confectionery product run a median of 7 months, so this one was shorter than usual for its category. Snacks and confectionery recall for allergens more than for anything else, because a chocolate or a coated snack passes through shared equipment carrying milk, soy and nuts, and the label is the only control between them and the consumer.
Filed under snacks and confectionery. A product can sit in more than one.
Other snacks and confectionery 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 Gedney Foods Product, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
All 3 records for Gedney Foods Product, LLC
All 2025 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.