Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent on customer
Summary
The FDA issued a Class I for Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent o by Wiers Farm Inc. Reason: Listeria monocyotgenes contamination.
Details
Source
Food Recall
External ID
F-1689-2024
Action Date
2024-08-14
Status
Terminated
Category
food
Product Description
Wiers Farm - Green Bell Pepper packaged into 1lb carton - cases size dependent on customer
Lot/Code Info: Lot No 240705, 240706, 240707, 240708, 240709, 240710, 240711, 240712
Quantity Affected: 14647 cases
Reason for Recall
Listeria monocyotgenes contamination
Distribution
CT, DE, IL, IN, KY, ME, MD, MI, MO, NJ, NY, NC, OH, PA, RI, TN, VA, WV
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-11
Company
Willard, OH
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 200 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wiers Farm Inc has 27 FDA actions in our database, including 27 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 (Wiers Farm Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wiers Farm Inc have FDA actions?
Wiers Farm Inc has 27 FDA actions in our database, including 27 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1689-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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