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RECALL RECORD — CLASS IRecall closedF-1876-2013/FDA enforcement
Saratoga Therapeutics, LLC·Dietary Supplements·Feb 13, 2013

Eba*(tm) Multivitamin Supplement, 180 Tablets in Plastic Bottles, Distributed by Saratoga…

What you need to know

Class I

  • What happened

    The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) despite labeling that incorrectly states it is free of milk components.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameSaratoga Therapeutics, LLC
Recalling firmSaratoga Therapeutics, LLCNorth Wales, PA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot number 0912164, exp 12/12 and 1110354, exp 10/14
Distribution area
Nationwide

Product was sold through physicians offices and via internet sales to consumers located nationwide and in Canada.

United States, Canada

Quantity affected890 bottles
Recall initiationFDA report date: September 11, 2013
FDA recall numberF-1876-2013

Beyond the headline

The recall, in context

Saratoga Therapeutics, LLC initiated this supplements recall on February 13, 2013. The FDA enforcement report states: The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) despite labeling that incorrectly states it is free of milk components. The FDA report lists distribution as: Product was sold through physicians offices and via internet sales to consumers located nationwide and in Canada.

The FDA enforcement report describes the reason as: The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) despite labeling that incorrectly states it is free of milk components.

Eba*(tm) Multivitamin Supplement, 180 Tablets in Plastic Bottles, Distributed by Saratoga… was made or distributed by Saratoga Therapeutics, LLC in North Wales, PA, United States. This page reflects FDA report F-1876-2013, dated September 11, 2013.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 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

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 Eba*(tm) Multivitamin Supplement, 180 Tablets in Plastic Bottles, Distributed by Saratoga… recall?

Saratoga Therapeutics, LLC recalled Eba*(tm) Multivitamin Supplement, 180 Tablets in Plastic Bottles, Distributed by Saratoga… in an FDA Class I enforcement action reported as F-1876-2013. The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) despite labeling that incorrectly states it is free of milk components.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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 Saratoga Therapeutics, LLC 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-1876-2013. 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.