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Geissler's Supermarket Recall: undeclared allergens (egg)

United States

TerminatedClass I

Company
Geissler's Supermarket
Product
Geissler's Supermarket Spicy Salmon 9.6 oz Ingredients read…
Recall date
March 28, 2024
Terminated
June 14, 2024
Source
FDA

Reason for recall

undeclared allergens (egg)

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Geissler's Supermarket Spicy Salmon 9.6 oz Ingredients read in part: "***INGREDIENTS:RICE, NORI, AVOCADO, SALMON, MAYONNAISE, CHILI, SUGAR, SALT, GARLIC, ACETIC ACID, POTASSIUM SORBATE, SODIUM Bl SULFITE, XANTHAN GUM, VINEGAR, ORANGE JUICE, ALCOHOL, HIGH FRUCTOSE CORN SYRUP, WATER, CITRIC ACID, SODIUM BENZOATE, SOY SAUCE(WATER, WHEAT, SOYBEAN, SALT, ALCOHOL), SOYPROTEIN, VINEGAR, SUGAR, SALT, SEAWEED, SESAME Oil, SESAME SEED, HORSERADISH, MUSTARD. KEEP REFRIGERATED. ***MADE IN A FACllllY THAT PROCESSES SHELLFISH, SOY, PEANUTS, TREE NUTS, EGGS, DAIRY & WHEAT***" Evaluation of this label found it does not declare egg in the mayonnaise sub ingredient. Hazard statement does not list sesame, does not list fish Not published in this source record 193 units total best by 03/27/24 or 03/28/24 UPC Codes: 234011006496

Distribution

  • CT & MA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1254-2024
Event ID
94311
Status
Terminated
Classification
Class I
Company
Geissler's Supermarket
Product description
Geissler's Supermarket Spicy Salmon 9.6 oz Ingredients read in part: "***INGREDIENTS:RICE, NORI, AVOCADO, SALMON, MAYONNAISE, CHILI, SUGAR, SALT, GARLIC, ACETIC ACID, POTASSIUM SORBATE, SODIUM Bl SULFITE, XANTHAN GUM, VINEGAR, ORANGE JUICE, ALCOHOL, HIGH FRUCTOSE CORN SYRUP, WATER, CITRIC ACID, SODIUM BENZOATE, SOY SAUCE(WATER, WHEAT, SOYBEAN, SALT, ALCOHOL), SOYPROTEIN, VINEGAR, SUGAR, SALT, SEAWEED, SESAME Oil, SESAME SEED, HORSERADISH, MUSTARD. KEEP REFRIGERATED. ***MADE IN A FACllllY THAT PROCESSES SHELLFISH, SOY, PEANUTS, TREE NUTS, EGGS, DAIRY & WHEAT***" Evaluation of this label found it does not declare egg in the mayonnaise sub ingredient. Hazard statement does not list sesame, does not list fish
Quantity
193 units total
Reason
undeclared allergens (egg)
Recall initiation date
March 28, 2024
Report date
May 29, 2024
Classification date
Not published in this source record
Termination date
June 14, 2024
Distribution pattern
CT & MA
UPC, lot, and code information
best by 03/27/24 or 03/28/24 UPC Codes: 234011006496
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 94311 with 5 other product entries in Public Health Trace.

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Distribution
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Published
May 29, 2024
Distribution
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Published
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Distribution
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Responsible company: Geissler's Supermarket

Other recalls from Geissler's Supermarket

FDA Recall United States Terminated Historical recordClass I

Geissler's Supermarket

Product
Geissler's Supermarket Shrimp Tempura and Lobster Roll 12 o…
Published
May 29, 2024
Distribution
CT & MA

View recall →

FDA Recall United States Terminated Historical recordClass I

Geissler's Supermarket

Product
Geissler's Supermarket Spicy Tuna (8) Ingredients read in p…
Published
May 29, 2024
Distribution
CT & MA

View recall →

FDA Recall United States Terminated Historical recordClass I

Geissler's Supermarket

Product
Geissler's Supermarket Shrimp Tempura and Spicy Shrimp Ing…
Published
May 29, 2024
Distribution
CT & MA

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
Connecticut 1
Massachusetts 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.