Skip to main content

Dierbergs Markets, Inc Corporate Office Recall: Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster).

United States

TerminatedClass I

Company
Dierbergs Markets, Inc Corporate Office
Product
Scampi Butter, Net Wt. 3 OZ, packaged in clear plastic tubs.…
Recall date
August 14, 2017
Terminated
September 19, 2017
Source
FDA

Reason for recall

Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster).

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Scampi Butter, Net Wt. 3 OZ, packaged in clear plastic tubs. Dierbergs Kitchens Not published in this source record 1,242 3 oz containers Sell-by dates 10/9/17 and earlier.

Distribution

  • Distributed to retail grocery stores in central and western Missouri and eastern Illinois.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-3558-2017
Event ID
77946
Status
Terminated
Classification
Class I
Company
Dierbergs Markets, Inc Corporate Office
Product description
Scampi Butter, Net Wt. 3 OZ, packaged in clear plastic tubs. Dierbergs Kitchens
Quantity
1,242 3 oz containers
Reason
Flavored butter contains undeclared fish (bonito and cod) and crustacean shellfish (shrimp, crab, and lobster).
Recall initiation date
August 14, 2017
Report date
September 27, 2017
Classification date
Not published in this source record
Termination date
September 19, 2017
Distribution pattern
Distributed to retail grocery stores in central and western Missouri and eastern Illinois.
UPC, lot, and code information
Sell-by dates 10/9/17 and earlier.
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

Other products recalled under this same event

This recall shares FDA event ID 77946 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Dierbergs Markets, Inc Corporate Office

Product
Cabernet Grille Butter, Net Wt. 3 OZ, packaged in clear plas…
Published
September 27, 2017
Distribution
Distributed to retail grocery stores in…

View recall →

Responsible company: Dierbergs Markets, Inc Corporate Office

Other recalls from Dierbergs Markets, Inc Corporate Office

FDA Recall United States Terminated Historical recordClass I

Dierbergs Markets, Inc Corporate Office

Product
Dierbergs Kitchen Salad Togo Classic Ham & Turkey Chef Salad…
Published
January 22, 2020
Distribution
Distributed to consumers at Dierbergs Ma…

View recall →

FDA Recall United States Terminated Historical recordClass I

Dierbergs Markets, Inc Corporate Office

Product
Dierbergs Kitchen Salad Togo Grilled Chicken Cobb Salad pac…
Published
January 22, 2020
Distribution
Distributed to consumers at Dierbergs Ma…

View recall →

FDA Recall United States Terminated Historical recordClass I

Dierbergs Markets, Inc Corporate Office

Product
Dierbergs Kitchen Remoulade packaged in 12 OZ containers, UP…
Published
January 22, 2020
Distribution
Distributed to consumers at Dierbergs Ma…

View recall →

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.