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Ducktrap River of Maine LLC Recall: Herring in Wine Sauce contains undeclared milk

United States

TerminatedClass I

Company
Ducktrap River of Maine LLC
Product
Ducktrap River of Maine Herring Center Cuts in Wine Sauce,…
Recall date
January 3, 2020
Terminated
March 30, 2020
Source
FDA

Reason for recall

Herring in Wine Sauce contains undeclared milk

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz. Not published in this source record 972 units SELL BY JUL 29, 2020; UPC 082674072408

Distribution

  • AL
  • GA
  • LA
  • ME
  • MA
  • MO
  • NH
  • NY
  • NC
  • OH
  • SC
  • TN
  • VT
  • VA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0633-2020
Event ID
84621
Status
Terminated
Classification
Class I
Company
Ducktrap River of Maine LLC
Product description
Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz.
Quantity
972 units
Reason
Herring in Wine Sauce contains undeclared milk
Recall initiation date
January 3, 2020
Report date
February 12, 2020
Classification date
Not published in this source record
Termination date
March 30, 2020
Distribution pattern
AL, GA, LA, ME, MA, MO, NH, NY, NC, OH, SC, TN, VT, VA
UPC, lot, and code information
SELL BY JUL 29, 2020; UPC 082674072408
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: Ducktrap River of Maine LLC

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
Alabama 1
Georgia 1
Louisiana 1
Maine 1
Massachusetts 1
Missouri 1
New Hampshire 1
New York 1
North Carolina 1
Ohio 1
South Carolina 1
Tennessee 1
Vermont 1
Virginia 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?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.