EveryPlate Meal Kit Product Codes 87-88-89-90-91-94-101 from Production Week 35 (production week start date: 08/25/2021)
Summary
The FDA issued a Class I for EveryPlate Meal Kit Product Codes 87-88-89-90-91-94-101 from Production Week 35 by HELLOFRESH US. Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak..
Details
Source
Food Recall
External ID
F-0205-2022
Action Date
2021-11-24
Status
Terminated
Category
food
Product Description
EveryPlate Meal Kit Product Codes 87-88-89-90-91-94-101 from Production Week 35 (production week start date: 08/25/2021)
Lot/Code Info: Production Week: 08/25/2021 EveryPlate Product Code: 87-88-89-90-91-94-101 (Number sequence may vary)
Quantity Affected: N/A
Reason for Recall
Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Distribution
Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-22
Company
New York, NY
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 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.
HELLOFRESH US has 18 FDA actions in our database, including 18 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 (HELLOFRESH US) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HELLOFRESH US have FDA actions?
HELLOFRESH US has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0205-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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