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Lower risk Food recall · FDA · Published March 16, 2016

Bumble Bee Chunk Light Tuna Recall: Process Deviations in Co-Pack Facility

Bumble Bee is recalling specific UPC codes of Chunk Light Tuna in Oil due to process deviations in a co-pack facility. Consumers should check UPC codes and best buy dates to determine if their product is affected.

🇺🇸 FDA recall #F-1072-2016FoodBumble Bee ›
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Recalling firmBumble Bee Foods LLC280 10th Ave · San Diego, CA 92101
✎ GovInfoNow plain-language explainer

What happened, in plain English

Bumble Bee is recalling certain cans of Chunk Light Tuna in Oil because of process deviations in a co-pack facility. This recall affects products with specific UPC codes and best buy dates from February 2019. The issue does not pose a direct health risk but requires consumers to check their product details. Read more at govinfonow.com/recall/25036-bumble-bee-chunk-light-tuna-recall-process-deviations-in-co.

Source Summary by GovInfoNow · govinfonow.com/recall/25036-bumble-bee-chunk-light-tuna-recall-process-deviations-in-co · Updated August 18, 2026 · FDA enforcement record: FDA #F-1072-2016

Cite this page

“Bumble Bee Chunk Light Tuna Recall: Process Deviations in Co-Pack Facility.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/25036-bumble-bee-chunk-light-tuna-recall-process-deviations-in-co. Based on FDA recall #F-1072-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1072-2016%22&limit=1).

Why it’s dangerous

The recall is due to process deviations that occurred in a co-pack facility not owned or operated by Bumble Bee Foods. This means the product was manufactured under different quality control standards than usual, but there is no indication of a direct health hazard.

Who’s affected

Consumers who purchased Bumble Bee Chunk Light Tuna in Oil with the specific UPC codes and best buy dates from February 2019 are affected. Those most at risk are individuals who have the recalled product in their homes.

How to tell if you have this one

Check for the UPC code TOODGSCEFB on the can. The product was sold with best buy dates starting February 23, 2019.

  • Brand
    Bumble Bee
  • Product
    Bumble Bee Foods LLC recalls Bumble Bee Chunk Light Tuna in Oil, 48cans/case, 5oz., UPC 8660000021
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Nationwide in US: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, ME, MI, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WI
Recall numberProduct, codes & lotsQuantity
F-1071-2016Bumble Bee Chunk Light Tuna in Water, 48cans/case, 5oz, UPC 8660000020; Can Codes: TOA2BSCAFB, TOA3BSCAFB, TOA4BSCAFB, TOA5BSCAFB, TOABBSCAFB, TOACBSCAFB, TOADBSCAFB, TOAEBSCAFB, TOG3BSCAFB, TOG4BSCAFB, TOH6BSCAFB, TOH7BSCAFB, TOHABSCAFB, TOHBBSCAFB, TOHCBSCAFB, TOHDBSCAFB, TOJ1BSCAFB, TOJ2BSCAFB, TOJ3BSCAFB, TOJ4BSCAFB, TON1BSCAFB, TON3BSCAFB, TOO1BSCAFB, TOO2BSCAFB, TOO3BSCAFB, TOO4BSCAFB, TOO5BSCAFB, TOOABSCAFB, TOOBBSCAFB, TOODBSCAFB, TOOEBSCAFB, TOOFBSCAFB, TOR1BSCAFB, TOR4BSCAFB, TOR5BSCAFB Best Buy Dates: 02/10/2019, 02/16/2019, 02/17/2019, 02/18/2019, 02/22/2019, 02/23/2019, 02/25/201910,448 cases
F-1072-2016Bumble Bee Chunk Light Tuna in Oil, 48cans/case, 5oz., UPC 8660000021; Can Codes: TOODGSCEFB Best Buy Dates: 02/23/2019410 cases
F-1073-2016Bumble Bee Chunk Light Tuna in Water, 6cans, 4pk, 5oz, UPC 8660000736; Can Codes: TOODGSCEFBTO9BBSCAFB, TO9DBSCAFB, TOA2BSCAFB, TON2BSCAFB, TON4BSCAFB, TON8BSCAFB, TONBBSCAFB, TONDBSCAFB, TONFBSCAFB, TOW1BSCAFB, TOW2BSCAFB, TOW3BSCAFB, TOW4BSCAFB, TOW5BSCAFB, TOWBBSCAFB, TOWEBSCAFB. Best Buy Dates: 02/9/2019, 02/10/2019, 02/22/2019, 02/29/2019.20,721 cases
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC code TOODGSCEFB and best buy dates from February 23, 2019 on the can.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 34 states.

Alaska: nationwideAKMaine: named in the noticeMEVermont: nationwideVTNew Hampshire: named in the noticeNHWashington: nationwideWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: named in the noticeRIMassachusetts: nationwideMAOregon: named in the noticeORNevada: nationwideNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: named in the noticeCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: named in the noticeCONebraska: nationwideNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: nationwideWVVirginia: named in the noticeVAMaryland: nationwideMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: nationwideNMKansas: named in the noticeKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “Nationwide in US: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, ME, MI, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Michigan, Mississippi, Missouri, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Mar 16, 201612. FDA classified it Class II: Apr 13, 201623. Published in FDA’s Enforcement Report: Apr 20, 201634. FDA terminated the recall: Aug 24, 201642016
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled product?

The recall does not require immediate action, but you should check your product details to confirm if it is affected.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1072-2016 (March 16, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1072-2016 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA