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RECALL RECORD — CLASS IRecall closedF-0820-2013/FDA enforcement
Baugher Enterprises, Incorporated·Food·Nov 4, 2010

Baugher's Apple Cider, One Gallon and Half Gallon Plastic Jugs, with Plastic Caps Labeled In…

What you need to know

Class I

  • What happened

    An unpasteurized apple cider product is potentially linked to foodborne illnesses in cases confirmed with E. coli 0157:H7.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDAIN, MD, PAMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameBaugher Enterprises, Incorporated
Recalling firmBaugher Enterprises, IncorporatedWestminster, MD, United States
UPC / barcodes
7 10372 33002 47 10372 33001 7
Lot / date codes
  • The products are not identified with lot numbers. The jugs are labeled with UPCs: 710372330024 710372330017
Distribution area
INMDPA

The product was sold to a distributor in MD and retailers in MD and the Gettysburg, PA area.

United States

Quantity affected14200 gallons total
Recall initiationFDA report date: December 19, 2012
FDA recall numberF-0820-2013

Beyond the headline

The recall, in context

Baugher Enterprises, Incorporated initiated this food recall on November 4, 2010. The FDA enforcement report states: An unpasteurized apple cider product is potentially linked to foodborne illnesses in cases confirmed with E. coli 0157:H7. The FDA report lists distribution as: The product was sold to a distributor in MD and retailers in MD and the Gettysburg, PA area.

The FDA enforcement report describes the reason as: An unpasteurized apple cider product is potentially linked to foodborne illnesses in cases confirmed with E. coli 0157:H7.

Baugher's Apple Cider, One Gallon and Half Gallon Plastic Jugs, with Plastic Caps Labeled In… was made or distributed by Baugher Enterprises, Incorporated in Westminster, MD, United States. This page reflects FDA report F-0820-2013, dated December 19, 2012.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, some E. coli strains produce toxins that can cause severe, sometimes bloody diarrhea.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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

E. coli

Symptoms to watch for

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

When symptoms may appear

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Higher-risk groups

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

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 Baugher's Apple Cider, One Gallon and Half Gallon Plastic Jugs, with Plastic Caps Labeled In… recall?

Baugher Enterprises, Incorporated recalled Baugher's Apple Cider, One Gallon and Half Gallon Plastic Jugs, with Plastic Caps Labeled In… in an FDA Class I enforcement action reported as F-0820-2013. An unpasteurized apple cider product is potentially linked to foodborne illnesses in cases confirmed with E. coli 0157:H7.

What are the symptoms of E. coli exposure?

Severe stomach cramps, diarrhea, vomiting and sometimes a low fever. Bloody diarrhea or signs of dehydration need prompt medical attention.

How quickly can E. coli symptoms appear?

Usually 3 to 4 days after exposure, with a range of roughly 1 to 10 days.

Who is most at risk from E. coli?

Young children, older adults, pregnant people and people with weakened immune systems are at higher risk of complications.

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

How do I get a refund from Baugher Enterprises, Incorporated?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0820-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Baugher Enterprises, Incorporated 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-0820-2013. 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.