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RECALL RECORD — CLASS IIRecall closedF-1772/FDA enforcement
S Bertram INC.·Food·May 23, 2012

Eden Quality Product Pasteurized Apple Juice from Concentrate Vitamin C Added in a 46 Fluid…

What you need to know

Class II

  • What happened

    Laboratory test results found the product has arsenic at a level of 36.4 parts per billion (ppb).

  • 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 FDADistribution not listedMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameS Bertram INC.
Recalling firmS Bertram INC.Linden, NJ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot number 20121212
Distribution area

Tri-state area of New Jersey, New York and Pennsylvania.

United States

Quantity affected169 cases each containing (12) 46 ounce cans
Recall initiationFDA report date: August 1, 2012
FDA recall numberF-1772

Beyond the headline

The recall, in context

S Bertram INC. initiated this food recall on May 23, 2012. The FDA enforcement report states: Laboratory test results found the product has arsenic at a level of 36.4 parts per billion (ppb). The FDA report lists distribution as: Tri-state area of New Jersey, New York and Pennsylvania.

The FDA enforcement report describes the reason as: Laboratory test results found the product has arsenic at a level of 36.4 parts per billion (ppb).

Eden Quality Product Pasteurized Apple Juice from Concentrate Vitamin C Added in a 46 Fluid… was made or distributed by S Bertram INC. in Linden, NJ, United States. This page reflects FDA report F-1772, dated August 1, 2012.

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 lot and date codes 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

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

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 Eden Quality Product Pasteurized Apple Juice from Concentrate Vitamin C Added in a 46 Fluid… recall?

S Bertram INC. recalled Eden Quality Product Pasteurized Apple Juice from Concentrate Vitamin C Added in a 46 Fluid… in an FDA Class II enforcement action reported as F-1772. Laboratory test results found the product has arsenic at a level of 36.4 parts per billion (ppb).

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. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the S Bertram 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-1772. 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.