Sweet Potatoes sold under the brand names: HEB CUT SWEET POTATOES IN LIGHT SYRUP NET WT. 29 OZ (1 LB 13 OZ) 822g MADE WI
Summary
The FDA issued a Class II for Sweet Potatoes sold under the brand names: HEB CUT SWEET POTATOES IN LIGHT SYRUP by Moody Dunbar Inc. Reason: During an internal investigation, the firm noticed that the Retort Chart was malfunctioning. No data was recorded during the production run..
Details
Source
Food Recall
External ID
F-0286-2024
Action Date
2023-10-25
Status
Ongoing
Category
food
Product Description
Sweet Potatoes sold under the brand names: HEB CUT SWEET POTATOES IN LIGHT SYRUP NET WT. 29 OZ (1 LB 13 OZ) 822g MADE WITH PRIDE AND CARE FOR HEB, SAN ANTONIO, TEXAS 78204 UPC 0 41220 45933 9 & SYSCO Classic Cut Sweet Potatoes NET WT/PESO NETO 108 OZ (6 LB 12 OZ) 3.06 kg DISTRIBUTED BY/DISTRIBUIDO POR SYSCO CORPORATION, HOUSTON, TEXAS 77677 UPC 0 74865 10724 2
Lot/Code Info: HEB - DK21J 4ALC6/ BEST BY OCT 2025 Sysco - DK21J49LC8 & DK21J49LC9
Quantity Affected: HEB - 105 cases/12/29oz cans + Sysco - 144cases/6/108oz cans
Reason for Recall
During an internal investigation, the firm noticed that the Retort Chart was malfunctioning. No data was recorded during the production run.
Distribution
Product was shipped to Florida, Texas and Virginia.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-10
Company
Johnson City, TN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 19 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Moody Dunbar Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Moody Dunbar Inc have FDA actions?
This is the only FDA action we have on record for Moody Dunbar Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0286-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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