Severity
Critical
CriticalClass ITerminated
FDA Food recall · Reported April 17, 2013
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8
The product may contain an undeclared allergen soy
New Chapter, Inc. recalled NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UP… — a critical-severity action.
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UP… was recalled by New Chapter, Inc. in April 17, 2013. Reason: The product may contain an undeclared allergen soy. Check the official notice for the remedy. Verify recall #F-1299-2013 with the FDA Food before acting.
The recall
New Chapter, Inc. issued this critical-severity FDA Food recall — The product may contain an undeclared allergen soy.
- Critical
- severity level
- Class I
- classification
- April 17, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1299-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1299-2013) was formally reported on April 17, 2013, with the manufacturer initiating the action on March 13, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. New Chapter, Inc. is listed as the recalling firm, operating out of Brattleboro, VT. Federal records list the affected scope as 1,004 bottles.
The documented reason for this recall is: The product may contain an undeclared allergen soy Distribution data in the federal record shows the product reached: AK, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, KS, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, SD, TN, TX, UT, VT, WA, WI. 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, 1 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.
Drugs & Medications recalls over time
Where this recall sits in its category — 14,048 drugs & medications recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 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
1,004 bottles
Related Recalls
6
1 from same agency
Product description
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8
Reason for recall
The product may contain an undeclared allergen soy
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | F-1299-2013 |
| Date reported | April 17, 2013 |
| Date initiated | March 13, 2013 |
| Recalling firm | New Chapter, Inc. |
| Firm location | Brattleboro, VT |
| Affected scope | 1,004 bottles |
| Distribution | AK, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, KS, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, SD, TN, TX, UT, VT, WA, WI |
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-1299-2013) 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? ▼
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8. Recalled by New Chapter, Inc.. Units affected: 1,004 bottles.
Why was this product recalled? ▼
The product may contain an undeclared allergen soy
Which agency issued this recall? ▼
This recall was issued by the FDA Food on April 17, 2013. Severity: Critical. Recall number: F-1299-2013.
Where was the recalled product distributed? ▼
Distribution: AK, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, KS, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, SD, TN, TX, UT, VT, WA, WI.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1299-2013) 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.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 17, 2013.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.