Class ITerminated in FDA datasetNov 16, 2012

Chicken of the Sea Solid White Tuna in Water

Recalling firm: Tri-Union Seafoods, L.L.C dba Chicken of the Sea.

Why it was recalled

Chicken of the Sea is recalling Solid White Tuna in Water because the product label has undeclared soy allergen.

Check the codes ↓

The exact product

Chicken of the Sea Solid White Tuna in Water, 7 oz., 48 cans per case (case: 6 sets of multi-unit packs of 8 cans each), UPC 4800000097, case UPC 4800076127.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Best By Date Can Code October 1 2016 BE11D ASWAP October 1 2016 BE11D ASWAP October 1 2016 BE14D ASWAP October 1 2016 BE14D ASWAP October 1 2016 BE15D ASWAP October 1 2016 BE15D ASWAP October 1 2016 BE1AD ASWAP October 1 2016 BE1BD ASWAP October 1 2016 BE1CD ASWAP October 1 2016 BE1CD ASWAP October 1 2016 BE1CD ASWAP October 1 2016 BE1DD ASWAP October 1 2016 BE1DD ASWAP October 1 2016 BE1ED ASWAP October 1 2016 BE1AD ASWAP October 1 2016 BE1ED ASWAP October 1 2016 BE1BD ASWAP October 1 2016 BE1CD ASWAP October 1 2016 BE1ED ASWAP October 1 2016 BE15D ASWAP October 1 2016 BE1BD ASWAP October 1 2016 BE1CD ASWAP October 1 2016 BE1DD ASWAP October 1 2016 BE1ED ASWAP October 10 2016 BEA1D ASWAP October 10 2016 BEA1D ASWAP October 10 2016 BEAED ASWAP October 11 2016 BEBAD ASWAP October 11 2016 BEB1D ASWAP October 11 2016 BEBDD ASWAP October 11 2016 BEB1D ASWAP October 11 2016 BEB2D ASWAP October 11 2016 BEB3D ASWAP October 11 2016 BEB3D ASWAP October 11 2016 BEB3D ASWAP October 11 2016 BEB3D ASWAP October 11 2016 BEB4D ASWAP October 11 2016 BEB5D ASWAP October 11 2016 BEB5D ASWAP October 11 2016 BEBAD ASWAP October 11 2016 BEBAD ASWAP October 11 2016 BEBAD ASWAP October 11 2016 BEBAD ASWAP October 11 2016 BEBBD ASWAP October 11 2016 BEBBD ASWAP October 11 2016 BEBCD ASWAP October 11 2016 BEBCD ASWAP October 11 2016 BEBDD ASWAP October 11 2016 BEBDD ASWAP October 11 2016 BEBDD ASWAP October 11 2016 BEBED ASWAP October 11 2016 BEBED ASWAP October 11 2016 BEBED ASWAP October 12 2016 BECCD ASWAP October 12 2016 BEC4D ASWAP October 12 2016 BECAD ASWAP October 12 2016 BECBD ASWAP October 12 2016 BECCD ASWAP October 12 2016 BEC1D ASWAP October 12 2016 BEC5D ASWAP October 12 2016 BECBD ASWAP October 12 2016 BECCD ASWAP October 2 2016 BE21D ASWAP October 2 2016 BE21D ASWAP October 2 2016 BE22D ASWAP October 2 2016 BE22D ASWAP October 2 2016 BE23D ASWAP October 2 2016 BE23D ASWAP October 2 2016 BE24D ASWAP October 2 2016 BE24D ASWAP October 2 2016 BE25D ASWAP October 2 2016 BE25D ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE2CD ASWAP October 2 2016 BE2DD ASWAP October 2 2016 BE21D ASWAP October 2 2016 BE25D ASWAP October 2 2016 BE2AD ASWAP October 2 2016 BE2DD ASWAP October 2 2016 BE22D ASWAP October 2 2016 BE22D ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE22D ASWAP October 2 2016 BE25D ASWAP October 2 2016 BE2AD ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE2CD ASWAP October 2 2016 BE2CD ASWAP October 2 2016 BE2DD ASWAP October 2 2016 BE2DD ASWAP October 2 2016 BE2ED ASWAP October 2 2016 BE21D ASWAP October 2 2016 BE2AD ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE2BD ASWAP October 2 2016 BE2CD ASWAP October 2 2016 BE2DD ASWAP October 2 2016 BE2ED ASWAP October 3 2016 BE31D ASWAP October 3 2016 BE31D ASWAP October 3 2016 BE31D ASWAP October 3 2016 BE31D ASWAP October 3 2016 BE31D ASWAP October 9 2016 BE93D ASWAP October 9 2016 BE93D ASWAP October 9 2016 BE95D ASWAP October 9 2016 BE9AD ASWAP October 9 2016 BE9AD ASWAP October 9 2016 BE9BD ASWAP October 9 2016 BE9BD ASWAP October 9 2016 BE91D ASWAP October 9 2016 BE92D ASWAP October 9 2016 BE93D ASWAP October 9 2016 BE93D ASWAP October 9 2016 BE94D ASWAP October 9 2016 BE94D ASWAP October 9 2016 BE95D ASWAP

Recall details

Recall number
F-0736-2013
Event ID
63699
FDA status
Terminated
Initiated
Nov 16, 2012
Reported
Dec 5, 2012
Classified
Nov 27, 2012
Terminated
Aug 6, 2013
Quantity
42,168 cases
Location
San Diego, CA, 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

Nationwide in the US: TX, IL, UT, WA, CA, AZ.

FDA source record · F-0736-2013

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.