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Stop using now Food recall · FDA · Published June 1, 2016

Aldi Millville Protein Chew Bars Recalled for Listeria Risk

Aldi's Millville peanut, dark chocolate & almond protein chew bars are recalled due to potential Listeria Monocytogenes contamination. Check your lot numbers.

🇺🇸 FDA recall #F-2083-2016FoodMillville ›
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Contact the company

Recalling firmSchulze & Burch Biscuit Co1133 W 35th St · Chicago, IL 60609-1447
✎ GovInfoNow plain-language explainer

What happened, in plain English

Schulze & Burch Biscuit Co is recalling Aldi's Millville protein chew bars because a supplier of one ingredient tested positive for Listeria Monocytogenes. This is a Class I recall, indicating the highest risk of serious adverse health consequences or death. The product was distributed to Aldi stores across the United States. Read more at govinfonow.com/recall/24190-aldi-millville-protein-chew-bars-recalled-for-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/24190-aldi-millville-protein-chew-bars-recalled-for-listeria-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-2083-2016

Cite this page

“Aldi Millville Protein Chew Bars Recalled for Listeria Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24190-aldi-millville-protein-chew-bars-recalled-for-listeria-risk. Based on FDA recall #F-2083-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2083-2016%22&limit=1).

Why it’s dangerous

The product may be contaminated with Listeria Monocytogenes, a bacterium that can cause serious infections. Infection can lead to symptoms such as fever, muscle aches, nausea, or diarrhea, and in severe cases, meningitis or septicemia, which can be fatal.

Who’s affected

Consumers who purchased Aldi's Millville protein chew bars (peanut, dark chocolate & almond) in yellow and brown boxes containing five bars each. Listeria Monocytogenes poses a serious health risk, particularly to pregnant women, older adults, and people with weakened immune systems.

How to tell if you have this one

Look for Aldi's Millville protein chew bars in yellow and brown boxes with brown and white lettering. Check the expiration dates on the packaging against this list: OCT14162T1, OCT15161T1, OCT15162T1, OCT28162T1, OCT29161T1, OCT29162T1, NOV08162T1, NOV09161T1, DEC04161T1, DEC04162T1, DEC18161T1, DEC18162T1, DEC31162T1, JAN01171T1, JAN01172T1, JAN14171T1, JAN14172T1, JAN15171T1, JAN20172T1, and JAN21171T1.

  • Brand
    Millville
  • Category
    Food
FDA recall event · 2 products

All 2 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 I
  • Status
    Terminated
  • Distribution
    The product was shipped to Aldi Inc. , 1200 Kirk Road, Batavia, IL 60510 from there it is further shipped to distribution centers andd then to Aldi stores. no product was distributed to foreign firms.
Recall numberProduct, codes & lots
F-2082-2016Aldi's Millville protein chew bars, dark chocolate peanut butter packaged 5 bars to a box in a yellow and brown box with brown and white lettering.; i. SEP14162T1 ii. OCT14161T1 iii. OCT14162T1 iv. OCT18162T1 v. OCT19161T1 vi. OCT19162T1 vii. OCT28161T1 viii. OCT28162T1 ix. NOV08161T1 x. NOV08162T1 xi. JAN01172T1 xii. JAN02171T1 xiii. JAN15171T1 xiv. JAN15172T1
F-2083-2016Aldi's Millville protein chew bars, peanut, dark chocolate & almond packaged 5 bars per box in a yellow and brown box with brown and white lettering.; i. OCT14162T1 ii. OCT15161T1 iii. OCT15162T1 iv. OCT28162T1 v. OCT29161T1 vi. OCT29162T1 vii. NOV08162T1 viii. NOV09161T1 ix. DEC04161T1 x. DEC04162T1 xi. DEC18161T1 xii. DEC18162T1 xiii. DEC31162T1 xiv. JAN01171T1 xv. JAN01172T1 xvi. JAN14171T1 xvii. JAN14172T1 xviii. JAN15171T1 xix. JAN20172T1 xx. JAN21171T1
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled protein chew bars if you have any of the listed expiration dates.

  2. Discard or return the item

    The recall record does not specify a remedy such as a refund or replacement, so consumers should dispose of the product to avoid ingestion.

Where it went and when

Where it was distributed

Distributed in Illinois, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “The product was shipped to Aldi Inc. , 1200 Kirk Road, Batavia, IL 60510 from there it is further shipped to distribution centers andd then to Aldi stores. no product was distributed to foreign firms.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois.

Recall timeline

FDA terminated this recall 3.2 years after the firm started it.

1. Firm started the recall: Jun 1, 201612. FDA classified it Class I: Sep 2, 201623. Published in FDA’s Enforcement Report: Sep 14, 201634. FDA terminated the recall: Aug 2, 2019420162019
  1. Firm started the recall
  2. FDA classified it Class I
  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

Where was this product sold?

The product was shipped to Aldi Inc. in Batavia, IL, and distributed to Aldi stores. No product was distributed to foreign firms.

How many cases were recalled?

Approximately 64,955 cases or 779,460 cartons (with 12 cartons per case) were involved in the recall.

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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-2083-2016 (June 1, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2083-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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