a.) King Kullen brand Pineapple Slices; UPC 85316-10007; 20 oz foam tray b) Wild By…
Gracie's Kitchens Inc. recalled this product and the FDA reported the enforcement action on 8 January 2025 as Class II. The recall was initiated by the firm. Product may be contaminated with Listeria monocytogenes.
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
- a.) King Kullen brand Pineapple Slices; UPC 85316-10007; 20 oz foam tray b) Wild By Nature brand Pineapple Slices; UPC: 85316-10007; 20 oz foam tray c.) King Kullen brand Pineapple Chunks; UPC: 85316-10386; 16 oz plastic container d.) King Kullen brand Pineapple Spears; UPC: 85316-10388; 16 oz plastic container e.) King Kullen brand Pineapple Slices; UPC: 85316-10542; 16 oz plastic container f.) Wild By Nature brand Pineapple Chunks; UPC: 85316-10380; 12 oz plastic container g.) Wild By Nature brand Pineapple Chunks: UPC: 85316-10386; 16 oz plastic container h.) Gracie's Kitchen brand Pineapple Spears; UPC: 85316-10341; 16 oz plastic container i.) Gracie's Kitchen brand Pineapple Chunks; UPC: 85316-10354; 16 oz plastic container j.) Gracie's Kitchen brand Pineapple Chunks; UPC: 85316-10380; 12 oz plastic container k.) Gracie's Kitchen brand Pineapple Cup; UPC: 85316-10386; 16 oz plastic container l.) King Kullen brand Pineapple Chunks; UPC: 85316-10380; 12 oz plastic container
- UPC
- 8531610007
- Reason for recall
- Product may be contaminated with Listeria monocytogenes.
- Recalling firm
- Gracie's Kitchens Inc.
- Firm location
- New Haven, Connecticut, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0324-2025
- Quantity
- 3681 cases total
- Distribution
- CT and NY
- Initiated
- 27 November 2024
- Reported by FDA
- 8 January 2025
- Terminated
- 10 April 2025
- Firm notified by
- Product codes
- a.) Sell By Dates: 11/09-11/19/24 b.) Sell By Dates: 11/09-11/19/24 c.) Sell By Dates: 11/11-11/21/24 d.) Sell By Dates: 11/11-11/21/24 e.) Sell By Dates: 11/9-11/19/24 f.) Sell By Dates: 11/11-11/21/24 g.) Sell By Dates: 11/11-11/21/24 h.) Sell By Dates: 11/11-11/21/24 i.) Sell By Dates: 11/11-11/21/24 j.) Sell By Dates: 11/11-11/21/24 k.) Sell By Dates: 11/11-11/21/24 i.) Sell By Dates: 11/11-11/21/24
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 34 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 34 separate recalls, which almost every published figure does, overstates it by a factor of 34. All 34 of them are listed on this page.
- The recall ran for 4 months, from 27 November 2024 to termination on 10 April 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 2 states, and the FDA published the enforcement report 6 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.
Named in the distribution pattern: Connecticut, New York. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Listeria monocytogenes
Listeria monocytogenes is a bacterium that grows at refrigeration temperature, which is why it dominates recalls of ready-to-eat foods that are never cooked again before they are eaten.
A preventive controls plan covers Listeria contamination under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(3)
- Sanitation controls: the controls on cleaning food-contact surfaces and on preventing cross-contact and cross-contamination from insanitary objects, people and equipment.
- 21 CFR 117.165(a)(3)
- Environmental monitoring: testing the processing environment for an environmental pathogen, required when a ready-to-eat food is exposed to the environment before packaging.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Every product in this recall
The FDA opened 34 enforcement records for this one recall, one per product code. This page carries all of them; the 33 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 Gracie's Kitchens Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 34 other records name this firm.
All 35 records for Gracie's Kitchens Inc.
All 2025 recalls · All FDA food recall data
21 CFR 117.135(c)(3) is the clause behind this recall, and it is one 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.