Summary
The FDA issued a Class I for HMC Farms Peaches Signature Farms 2lb bag by The HMC Group Marketing Inc. Reason: Potential contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0648-2024
Action Date
2023-12-27
Status
Terminated
Category
food
Product Description
HMC Farms Peaches Signature Farms 2lb bag
Lot/Code Info: STN #6359
Quantity Affected: not available
Reason for Recall
Potential contamination with Listeria monocytogenes
Distribution
U.S. distribution to the following: CA, OR, MA, PA, AK, WA, CO, UT, TN, MO, IL, MN, VA, KS, NC, TX, AZ, GA, OH, NY, NJ, ID, WI, FL, SC, AL, NV Foreign distribution to the following: Mexico, Canada, and Taiwan
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-17
Company
Kingsburg, 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 157 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The HMC Group Marketing Inc 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 (The HMC Group Marketing Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The HMC Group Marketing Inc have FDA actions?
The HMC Group Marketing Inc 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 "F-0648-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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