Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid. Be
Summary
The FDA issued a Class I for Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with by Epicurean Butter Co.. Reason: Firm's supplier of frozen dill notified firm of a recall due to potential contamination with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1584-2022
Action Date
2022-09-07
Status
Terminated
Category
food
Product Description
Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid. Best By and Lot # printed with blue ink by the label around the cup. UPC 0 77890 44324 8. Distributed By: Wegman Food Markets Inc. Rochester, NY 14603 Keep Refrigerated. Note: There are 8 cups in a mastercase.
Lot/Code Info: Lot # Expiration Date 16314 07/05/22 16357 07/16/22 16438 07/21/22 16536 08/09/22 16619 08/24/22 16702 09/14/22 16722 09/15/22 16761 09/22/22 16797 09/30/22 16829 10/06/22 16902 10/18/22 17037 11/17/22
Quantity Affected: 1137 cases
Reason for Recall
Firm's supplier of frozen dill notified firm of a recall due to potential contamination with Listeria monocytogenes.
Distribution
Wegmans Food Markets in MA, MD, NC, NJ, NY, PA, VA, DC.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-15
Company
Thornton, CO
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 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Epicurean Butter Co.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Epicurean Butter Co. have FDA actions?
This is the only FDA action we have on record for Epicurean Butter Co. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1584-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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