Class ITerminated in FDA datasetOct 28, 2025

PEACHES PRODUCE OF U.S.A. NET WT 2 LB (32 OZ) 907 g

Recalling firm: Moonlight Packing Corporation

Why it was recalled

Potential contamination with Listeria monocytogenes.

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

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

TypeCode / valueContext
UPC011110181749OZ) 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
UPC898429002091UPC 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 U

Recall details

Recall number
H-0316-2026
Event ID
97908
FDA status
Terminated
Initiated
Oct 28, 2025
Reported
Dec 17, 2025
Classified
Dec 17, 2025
Terminated
Jul 31, 2026
Quantity
46,048 cases (12-2 lb. bags/case)
Location
Reedley, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

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

FDA source record · H-0316-2026

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.