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RECALL RECORD — CLASS IIRecall closedF-1321-2013/FDA enforcement
Sib, INC.·Food·Mar 25, 2013

Bakehouse Granola, 12 OZ, 340 g Scholar's Inn Bakehouse Granola 16 OZ, 454 g All Natural, Baked…

What you need to know

Class II

  • What happened

    Bake House Granola, does not list the source of the unsalted butter ingredient as milk, an allergen. People who have an allergy or severe sensitivity to milk, run the risk of…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameSib, INC.
Recalling firmSib, INC.Bloomington, IN, United States
UPC / barcodes
0 063565 50752 46 35655 00524 9
Lot / date codes
  • 12 oz bags: UPC 0063565507524, Best by 5/14/13-7/1/13 Lots 213A, 213B, 214A, 214B, 216A, 216B, 217A, 217B, 220B, 221A, 221B, 224B, 226A, 226B, 227A, 227B, 228A, 228B, 307A, 307B, 308A, 313A, 313B, 314A, 314B, 316A, 316B, 320A, 320B, 321A, 321B, 323A, and 323BC 16oz bags: UPC: 635655005249 Best by: 3/9/13 -5/9/13 Lots 1209A, 1209B, 1209AB, 1209BB, 1210A, 1210B, 1210AB, 1210 BB, 108A, 108B, 113A, 113 B, 116A, 116B, 117A, 117B, 118A, 118B, 123A, 123B, 124A, 124B, 130A, 203A, 203B, 131A, 131B, 206A, 206B, 207A, 207B, 209A, 209B, and 209C
Distribution area
IN

retail grocery stores in Indiana and 1 retail store in Illinois

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: May 1, 2013
FDA recall numberF-1321-2013

Beyond the headline

The recall, in context

Sib, INC. initiated this food recall on March 25, 2013. The FDA enforcement report states: Bake House Granola, does not list the source of the unsalted butter ingredient as milk, an allergen. People who have an allergy or severe sensitivity to milk, run the risk of serious or life-threatening allergic reaction if they consume these products. The FDA report lists distribution as: retail grocery stores in Indiana and 1 retail store in Illinois.

The FDA enforcement report describes the reason as: Bake House Granola, does not list the source of the unsalted butter ingredient as milk, an allergen. People who have an allergy or severe sensitivity to milk, run the risk of serious or life-threatening allergic reaction if they consume these products.

Bakehouse Granola, 12 OZ, 340 g Scholar's Inn Bakehouse Granola 16 OZ, 454 g All Natural, Baked… was made or distributed by Sib, INC. in Bloomington, IN, United States. This page reflects FDA report F-1321-2013, dated May 1, 2013.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Bakehouse Granola, 12 OZ, 340 g Scholar's Inn Bakehouse Granola 16 OZ, 454 g All Natural, Baked… recall?

Sib, INC. recalled Bakehouse Granola, 12 OZ, 340 g Scholar's Inn Bakehouse Granola 16 OZ, 454 g All Natural, Baked… in an FDA Class II enforcement action reported as F-1321-2013. Bake House Granola, does not list the source of the unsalted butter ingredient as milk, an allergen. People who have an allergy or severe sensitivity to milk, run the risk of…

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Sib, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1321-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.