Class IITerminated in FDA datasetRecall initiated Aug 15, 2019

Grained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigerated, packed in a metal tin with…

Recalling firm: AWERS Inc

Why it was recalled

Grained salmon caviar, refrigerated, was recalled due to a potential to be contaminated with Clostridium botulinum.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 13, 2019.

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Compare the exact product and package details with the label you have.

ProductGrained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigerated, packed in a metal tin with Cyrillic lettering. The tin is green, with red and white writing with an easy open pull lid. UPC 8 85202 00044 3. The label is read in parts: "***GRAINED SALMON CAVIAR ***INGREDIENTS: RED SALMON (FISH) ROE, SALT, SORBIC ACID TO PROTECT FRESHNESS*** KEEP REFRIGERATED AT 32 F OR COOLER***Manufactured by AWERS INC., Bellevue, WA***".
Package size95g
UPC885202000443

FDA code information

BEST BEFORE JUL 03 2020. BEST BEFORE JUL 15 2020. BEST BEFORE SEP 17 2020. BEST BEFORE OCT 07 2020. BEST BEFORE OCT 13 2020.

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Full FDA record and distribution details

Original product description

Grained Salmon Caviar 95g (Sockeye Salmon Caviar), refrigerated, packed in a metal tin with Cyrillic lettering. The tin is green, with red and white writing with an easy open pull lid. UPC 8 85202 00044 3. The label is read in parts: "***GRAINED SALMON CAVIAR ***INGREDIENTS: RED SALMON (FISH) ROE, SALT, SORBIC ACID TO PROTECT FRESHNESS*** KEEP REFRIGERATED AT 32 F OR COOLER***Manufactured by AWERS INC., Bellevue, WA***".

Extracted codes and context

TypeCode / valueContext
UPC885202000443. The tin is green, with red and white writing with an easy open pull lid. UPC 8 85202 00044 3. The label is read in parts: "***GRAINED SALMON CAVIAR ***INGREDIENTS: RED SALMON (FISH) ROE, SALT, SORBIC ACID TO P

Original FDA recall reason

Grained salmon caviar, refrigerated, was recalled due to a potential to be contaminated with Clostridium botulinum.

Recall details

Recall number
F-2094-2019
Event ID
83585
FDA status
Terminated
Initiated
Aug 15, 2019
Reported
Sep 4, 2019
Classified
Aug 29, 2019
Terminated
Nov 13, 2019
Quantity
Total 4,288 cans
Location
Bellevue, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed in California, New York, Oregon Washington, and Canada. Product was further distributed to Illinois and product may have further distributed to other states.

FDA source record · F-2094-2019

Data updated September 16, 2026. View official FDA data ↗

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