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FDA FOOD RECALLS

Look up any food recall

Every FDA food recall since 2012, in one place. We check each recall's status with FDA every day.

Checked with FDA daily · Source: U.S. Food and Drug Administration

550 recalls · showing 441 to 460

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  1. ENDEDClass II · ModerateRecalled Jul 6, 2016

    MOZZARELLA CALZONE, 100 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.

    Product was manufactured with flour recalled due to E. coli O121 contamination.

    Kabobs Inc · Lake City, GA

    Where it was sold: AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, LA, MA, MD, MI, MN, MO, NC, NJ, NY, NV, OK, OH, OR, PA, TN, TX WA, and WI.

    Show details
    Product, as FDA describes it
    MOZZARELLA CALZONE, 100 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
    Reason, in FDA's words
    Product was manufactured with flour recalled due to E. coli O121 contamination.
    Codes on the package
    Item number: K8871, Lot/Julian Code: PM15M08 / 15342.
    Where it was sold
    AR, CA, CO, CT, FL, GA, IL,IN, IO, KY, LA, MA, MD, MI, MN, MO, NC, NJ, NY, NV, OK, OH, OR, PA, TN, TX WA, and WI.
    Amount recalled
    23 cases/7 cases (100 units per case).
    Status
    Ended Nov 6, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0145-2017
    View in FDA's recall database
  2. ENDEDClass I · Most seriousRecalled Jul 6, 2016

    Tortilla Crusted Crumb is a breading system. Product Item Key N21997-B. It composed of flour and ot...

    Tortilla Crusted Crumb is recalled due to a potential to be contaminated with E. coli O121.

    Hydroblend Inc · Nampa, ID

    Where it was sold: distributed in WA.

    Show details
    Product, as FDA describes it
    Tortilla Crusted Crumb is a breading system. Product Item Key N21997-B. It composed of flour and other food grade ingredients. Product is bagged in 25 lbs. multiwalled polylined paper bags.
    Reason, in FDA's words
    Tortilla Crusted Crumb is recalled due to a potential to be contaminated with E. coli O121.
    Codes on the package
    Lot# 0016335
    Where it was sold
    distributed in WA.
    Amount recalled
    2575 lbs.
    Status
    Ended Aug 15, 2016 (FDA lists it as terminated)
    FDA recall number
    F-1874-2016
    View in FDA's recall database
  3. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Man...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31800
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    40,080 lbs
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0191-2017
    View in FDA's recall database
  4. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Carrot 281, Product Code 22281. 50 lb corrugated case with polyliner. Manufactured by: QualiTe...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Carrot 281, Product Code 22281. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31717, 31832
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    40,150 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0192-2017
    View in FDA's recall database
  5. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Bacon 286, Product Code 22286. 50 lb corrugated case with polyliner. Manufactured by: QualiTec...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Bacon 286, Product Code 22286. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot 31790
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    400 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0193-2017
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Jalapeno 321A, Product Code 22321A. 50 lb corrugated case with polyliner. Manufactured by: Qua...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Jalapeno 321A, Product Code 22321A. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lots: 31664, 31794, 31930
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    2,350 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0194-2017
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured b...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot 31483
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    300 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0195-2017
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: ...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot codes: 31476, 31802
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    6,000 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0196-2017
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Spinach 352, Product Code 22352. 50 lb corrugated case with polyliner. Manufactured by: QualiT...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Spinach 352, Product Code 22352. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lots: 31679, 31991
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    4,950 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0197-2017
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Cheddar Cheese, Product Code 22518. 50 lb corrugated case with polyliner. Manufactured by: Qua...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Cheddar Cheese, Product Code 22518. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lots: 31541, 31823, 31667, 31861
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    7,050 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0198-2017
    View in FDA's recall database
  11. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Red Bell Pepper, Product Code 22708. 50 lb corrugated case with polyliner. Manufactured by: Qu...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Red Bell Pepper, Product Code 22708. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lots: 31755, 32072
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    4,150 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0199-2017
    View in FDA's recall database
  12. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Jalapeno 709, Product Code 22709. 50 lb corrugated case with polyliner. Manufactured by: Quali...

    Quali Tech has been notified by a supplier that they received material with the potential presence of E. coli O 121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Jalapeno 709, Product Code 22709. 50 lb corrugated case with polyliner. Manufactured by: Quali Tech, 318 Hazel tine Drive, Chasma, MN 55318 USA
    Reason, in FDA's words
    Quali Tech has been notified by a supplier that they received material with the potential presence of E. coli O 121 bacteria.
    Codes on the package
    Lots: 31504, 31756
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    3,200 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0200-2017
    View in FDA's recall database
  13. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Rainbow Blend 714, Product Code 22714. 50 lb corrugated case with polyliner. Manufactured by: ...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Rainbow Blend 714, Product Code 22714. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lots: 31584, 31665, 31841, 31842
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    67,500 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0201-2017
    View in FDA's recall database
  14. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: ...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lots: 31624, 31978
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    1.500 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0202-2017
    View in FDA's recall database
  15. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: Qua...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31645, 31643
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    400 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0203-2017
    View in FDA's recall database
  16. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Bacon, Product Code 22763. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 3...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Bacon, Product Code 22763. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31750
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    50 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0204-2017
    View in FDA's recall database
  17. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Rainbow Blend, Product Code 22795. 50 lb corrugated case with polyliner. Manufactured by: Qual...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Rainbow Blend, Product Code 22795. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31950
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    1,400 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0205-2017
    View in FDA's recall database
  18. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Bacon, Product Code 24117. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 3...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Bacon, Product Code 24117. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31769
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    500 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0206-2017
    View in FDA's recall database
  19. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    FE Maple, Product Code 27128. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 3...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    FE Maple, Product Code 27128. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31552, 31939, 31969
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    32,750 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0207-2017
    View in FDA's recall database
  20. ENDEDClass I · Most seriousRecalled Jul 5, 2016

    PE Blueberry, Product Code 27136. 50 lb corrugated case with polyliner. Manufactured by: QualiTec...

    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.

    QualiTech, Inc · Chaska, MN

    Where it was sold: AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.

    Show details
    Product, as FDA describes it
    PE Blueberry, Product Code 27136. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Reason, in FDA's words
    QualiTech has been notified by a supplier that they received material with the potential presence of E. coli O121 bacteria.
    Codes on the package
    Lot: 31591, 31779, 31960
    Where it was sold
    AZ, CA, GA, ID, IL, IN, MI, MN, TX, WA. Outside the US to include: Canada.
    Amount recalled
    176,900 lbs.
    Status
    Ended Sep 13, 2017 (FDA lists it as terminated)
    FDA recall number
    F-0208-2017
    View in FDA's recall database

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What the classes mean

Class I · Most serious. FDA's highest level: products that could cause serious health problems or death.

Class II · Moderate. It may cause temporary health problems, or the risk of serious harm is remote.

Class III · Low risk. Not likely to cause health problems, but it breaks a labeling or manufacturing rule.

If you have a recalled product

  1. Match the codes on your package to the recall.
  2. If they match, don't eat it.
  3. Return it to the store or throw it away, as the company directs.
  4. If you feel sick, contact your doctor.

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Recall information comes from FDA's enforcement reports through openFDA. FDA publishes new reports weekly; we check every recall's status daily. This page is for information only and is not medical advice. Meat, poultry and egg products are recalled by USDA, not FDA, and are not listed here.