Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported September 11, 2013
ebA*(TM) Multivitamin Supplement, 180 tablets in plastic bottles, Distributed by Saratoga Therapeutics, LLC, North Wales, PA.
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.
Saratoga Therapeutics, LLC recalled ebA*(TM) Multivitamin Supplement, 180 tablets in plastic bottles, Distributed by Saratoga… - a critical-severity action.
ebA*(TM) Multivitamin Supplement, 180 tablets in plastic bottles, Distributed by Saratoga… was recalled by Saratoga Therapeutics, LLC in September 11, 2013. Reason: The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) de…. Check the official notice for the remedy. Verify recall #F-1876-2013 with the FDA Food before acting.
The recall
Saratoga Therapeutics, LLC issued this critical-severity FDA Food recall-The recall was initiated due to discovery of the presence of milk components (milk protein(s) and lactose) de….
- Critical
- severity level
- Class I
- classification
- September 11, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1876-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1876-2013) was formally reported on September 11, 2013, with the manufacturer initiating the action on February 13, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Saratoga Therapeutics, LLC is listed as the recalling firm, operating out of North Wales, PA. Federal records list the affected scope as 890 bottles.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Product was sold through physicians offices and via internet sales to consumers located nationwide and in Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
890 bottles
Related Recalls
6
6 from same agency
Product description
ebA*(TM) Multivitamin Supplement, 180 tablets in plastic bottles, Distributed by Saratoga Therapeutics, LLC, North Wales, PA.
Reason for recall
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1876-2013 |
| Date reported | September 11, 2013 |
| Date initiated | February 13, 2013 |
| Recalling firm | Saratoga Therapeutics, LLC |
| Firm location | North Wales, PA |
| Affected scope | 890 bottles |
| Distribution | Product was sold through physicians offices and via internet sales to consumers located nationwide and in Canada. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1876-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
ebA*(TM) Multivitamin Supplement, 180 tablets in plastic bottles, Distributed by Saratoga Therapeutics, LLC, North Wales, PA.. Recalled by Saratoga Therapeutics, LLC. Units affected: 890 bottles.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 11, 2013. Severity: Critical. Recall number: F-1876-2013.
Where was the recalled product distributed? ▼
Distribution: Product was sold through physicians offices and via internet sales to consumers located nationwide and in Canada..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1876-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported September 11, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.