$7 Crab Cake Meal packaged in a 3 compartment plastic container. 14oz, UPC 2 07879400700 8. Refrigerated product.
Summary
The FDA issued a Class I for $7 Crab Cake Meal packaged in a 3 compartment plastic container. 14oz, UPC 2 by Weis Markets, Inc., Ice Cream Division. Reason: Undeclared milk.
Details
Source
Food Recall
External ID
F-0960-2021
Action Date
2021-09-22
Status
Terminated
Category
food
Product Description
$7 Crab Cake Meal packaged in a 3 compartment plastic container. 14oz, UPC 2 07879400700 8. Refrigerated product.
Lot/Code Info: Sell by 8/25/2021 through 9/05/2021
Quantity Affected: 35 units
Reason for Recall
Undeclared milk
Distribution
Distributed to retail locations in MD, PA, NJ, and WV
Type: Voluntary: Firm initiated
Recall Initiated: 2021-09-01
Company
Sunbury, PA
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 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Weis Markets, Inc., Ice Cream Division has 6 FDA actions in our database, including 6 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 (Weis Markets, Inc., Ice Cream Division) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Weis Markets, Inc., Ice Cream Division have FDA actions?
Weis Markets, Inc., Ice Cream Division has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0960-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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