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WEIS MARKETS Recall: The ingredient label failed to declare egg because the store-made coleslaw scale label did not list the sub-ingredients of mayonnaise.

United States

TerminatedClass I

Company
WEIS MARKETS
Product
Cole Slaw, Store Made. Packed in deli-style plastic containe…
Recall date
March 21, 2018
Terminated
October 12, 2018
Source
FDA

Reason for recall

The ingredient label failed to declare egg because the store-made coleslaw scale label did not list the sub-ingredients of mayonnaise.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Cole Slaw, Store Made. Packed in deli-style plastic containers: Weis, Weis Markets, Inc., Sunbury, PA; Cabbage, Carrots, Pineapple, White Onions, Sugar, Salt Pepper, Vinegar, Hellmanns Mayonnaise Not published in this source record ~560 containers Sell By: Mar 21, 2018 thru Mar 24, 2018

Distribution

  • NY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0997-2018
Event ID
79599
Status
Terminated
Classification
Class I
Company
WEIS MARKETS
Product description
Cole Slaw, Store Made. Packed in deli-style plastic containers: Weis, Weis Markets, Inc., Sunbury, PA; Cabbage, Carrots, Pineapple, White Onions, Sugar, Salt Pepper, Vinegar, Hellmanns Mayonnaise
Quantity
~560 containers
Reason
The ingredient label failed to declare egg because the store-made coleslaw scale label did not list the sub-ingredients of mayonnaise.
Recall initiation date
March 21, 2018
Report date
April 4, 2018
Classification date
Not published in this source record
Termination date
October 12, 2018
Distribution pattern
NY
UPC, lot, and code information
Sell By: Mar 21, 2018 thru Mar 24, 2018
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: WEIS MARKETS

Other recalls from WEIS MARKETS

FDA Recall United States Terminated Historical recordClass I

WEIS MARKETS

Product
Dried Beef Party Rye Dip; Ingredients: Hellman's Mayonaise,…
Published
March 28, 2018
Distribution
NY and PA

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FDA Recall United States Terminated Historical recordClass I

WEIS MARKETS

Product
Weis Sunbury, PA 17801; Penne W/Asiago Sauce And Grilled Chi…
Published
March 28, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

WEIS MARKETS

Product
Weis Weis Markets, Inc., Sunbury, PA 17801-0471; Keep Refrig…
Published
February 21, 2018
Distribution
PA and NY

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
New York 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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