Dill Pickles packaged under the following label: 1. Gedney Whole Pickles, item 15100…
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
- Dill Pickles packaged under the following label: 1. Gedney Whole Pickles, item 15100, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00151 8. 2. Gedney Mini Munchers Kosher Dill, item 17100, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00171 6. 3. Gedney Kosher Dill Babies, item 17200, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00172 3. 4. Gedney Dill Mini Munchers, item 17300, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00173 0. 5. Gedney Dill Babies, item 18400, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00184 6. 6. Gedney Dill Babies, item 19100, Net 16 fl oz. (1Pt)473mL. UPC 0 41660-00191 4. 7. Gedney Kosher Dill Babies, item 19200, Net 32 fl oz. (1Qt)946mL. UPC 0 41660-00192 1. 8. Gedney Dill Spears, item 19600, 24 fl oz. (1Pt 8fl oz) 710mL. UPC 0 41660- 00196 9. Refrigerate after opening. Distributed by: Gedney Foods Co., Burnsville, MN 55337. Product of Mexico
- UPC
- 041660001518
- 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-0328-2025
- Quantity
- 3520 cases (each case contains 12 units)
- Distribution
- MN
- Initiated
- 9 June 2025
- Reported by FDA
- 30 July 2025
- Terminated
- 14 August 2025
- Firm notified by
- Letter
- Product codes
- 1. Lot Codes: 4364, 4267, 2. Lot Codes: 4268, 4281, 4309. 3. Lot Codes: 4268, 4285, 4288, 4292, 4296, 4302, 4306. 4. Lot Codes: 4264, 4271, 4274, 4278. 5. Lot Codes: 4264, 4313. 6. Lot Codes: 44271, 4274, 4278, 4281. 7. Lot Codes: 4309.
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. All 3 of them are listed on this page.
- 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.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Every product in this recall
The FDA opened 3 enforcement records for this one recall, one per product code. This page carries all of them; the 2 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-07-30 | 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. | Gedney Foods Product, LLC | Products were slated for disposal due to product and container damage, but were inadvertently sold. | Class II |
| 2025-07-30 | Gedney Ghost Pepper LIL Pickles, item 75802, Net 24 fl oz. (1.5Pts) 710mL. UPC 0 41660-00758 9. Refrigerate after opening. Distributed by Gedney Foods Co, Burnsville, MN 55438 Product of Mexico. | Gedney Foods Product, LLC | Products were slated for disposal due to product and container damage, but were inadvertently sold. | Class II |
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.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2025-07-30 | 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. | Gedney Foods Product, LLC | Products were slated for disposal due to product and container damage, but were inadvertently sold. | Class II |
| 2025-07-30 | Gedney Ghost Pepper LIL Pickles, item 75802, Net 24 fl oz. (1.5Pts) 710mL. UPC 0 41660-00758 9. Refrigerate after opening. Distributed by Gedney Foods Co, Burnsville, MN 55438 Product of Mexico. | Gedney Foods Product, LLC | Products were slated for disposal due to product and container damage, but were inadvertently sold. | Class II |
All 3 records for Gedney Foods Product, LLC
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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.