UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBUTED BY MOONLIGHT PACKING CORP. REEDLEY,
Summary
The FDA issued a Class I for UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBU by Moonlight Packing Corporation. Reason: Potential contamination with Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0316-2026
Action Date
2025-12-17
Status
Completed
Category
food
Product Description
UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g DISTRIBUTED BY MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654 UPC 0 11110 18174 9 PEACHES PRODUCE OF USA NET WT 32 OZ (2 LB) 907g DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202
Lot/Code Info: Lots: 01PCLC, 03PCAF, 106PCLF, 113PCAF, 113PCLF, 129PCLF, 134PCLF, 142PCLF, 150PCLF, 151PCLF, 159PCABA, 159PCABB, 159PCPG10, 20, 22PCAB, 22PCPG10A, 22PCPG10B, 22PCP8A, 22PCPG8B, 22PCPG8C, 23, 25, 30PCEN, 40LT, 40YP#3, 44PCLC, 44PCLCB, 45, 51PCLC, 51PCLCB, 86PCAF, 69PWPR, 79PWPRT
Quantity Affected: 46,048 cases (12-2 lb. bags/case)
Reason for Recall
Potential contamination with Listeria monocytogenes.
Distribution
Domestic: AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MN, MO, MS, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY Foreign: Canada, Mexico
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-28
Company
Reedley, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 105 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Moonlight Packing Corporation has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Moonlight Packing Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Moonlight Packing Corporation have FDA actions?
Moonlight Packing Corporation has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0316-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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