Class IITerminated · reported 2025-07-30

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.
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.

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 access

Recall 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.