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ModerateClass IITerminated

FDA Food recall · Reported August 12, 2020

Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product names, packaged in white plastic bottle with black plastic lid: 1. Aspire Rejuvenation Nutraceuticals, Tranquility PM, Mfg for: Aspire Rejuvenation Nutraceuticals, 74550 Dr Phillips Blvd Ste 205, Orlando, FL 32819. 2. Living Well Clinical Nutrition Center, SleepForce, Manufactured for: living Well Clinical Nutrition, 815 E. Main St Ste A, League City, TX 77573. 3.

Various branded dietary supplements may contain undeclared soy.

Recall #
F-1049-2020
Affected scope
95 bottles
Initiated
July 16, 2020
Verify with FDA Food →
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Provident Nutraceutical div. of Ortho Molecular Products Inc recalled Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the … - a moderate-severity action.

Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the … was recalled by Provident Nutraceutical div. of Ortho Molecular Products Inc in August 12, 2020. Reason: Various branded dietary supplements may contain undeclared soy.. Check the official notice for the remedy. Verify recall #F-1049-2020 with the FDA Food before acting.

The recall

Provident Nutraceutical div. of Ortho Molecular Products Inc issued this moderate-severity FDA Food recall-Various branded dietary supplements may contain undeclared soy..

Moderate
severity level
Class II
classification
August 12, 2020
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1049-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1049-2020) was formally reported on August 12, 2020, with the manufacturer initiating the action on July 16, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Provident Nutraceutical div. of Ortho Molecular Products Inc is listed as the recalling firm, operating out of Stevens Point, WI. Federal records list the affected scope as 95 bottles.

The documented reason for this recall is: Various branded dietary supplements may contain undeclared soy. Distribution data in the federal record shows the product reached: CA, FL, OH, TX, WA. 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 - 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.

Children & Baby Products recalls over time

Where this recall sits in its category - 3,731 children & baby products recalls on record

0100200300400500600 20052008201120142017202020232026 146
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

95 bottles

Related Recalls

6

0 from same agency

Product description

Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product names, packaged in white plastic bottle with black plastic lid: 1. Aspire Rejuvenation Nutraceuticals, Tranquility PM, Mfg for: Aspire Rejuvenation Nutraceuticals, 74550 Dr Phillips Blvd Ste 205, Orlando, FL 32819. 2. Living Well Clinical Nutrition Center, SleepForce, Manufactured for: living Well Clinical Nutrition, 815 E. Main St Ste A, League City, TX 77573. 3. Swiss Rx Superior Human Performance, Nighttime, Manufactured for Swiss Rx, 1668 Valtec LN STE H, Boulder, CO 80301. 4. energy health, Neuro Calm PM, Mfg for: Energy Health, 709 W. Leuda St., Fort Worth, TX 76104. 5. Nutra Molecular, Nutra Calm PM, Manufactured for: Nutra Molecular, 1543 S Bowen Rd, Pantego, TX 76013. 6. Good Medicine NeuroSleep, Manufactured for: Good Medicine, 5235 Morning Sun Rd, Oxford, OH 45056. 7. WiseMeds Tranquil PM + GABA, Neurotransmitter Support for a Healthy Sleep Cycle. Distributed by: WiseMeds, 534 S. Chickasaw Trail, Orlando, FL 32825. .

Reason for recall

Various branded dietary supplements may contain undeclared soy.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-1049-2020
Date reported August 12, 2020
Date initiated July 16, 2020
Recalling firm Provident Nutraceutical div. of Ortho Molecular Products Inc
Firm location Stevens Point, WI
Affected scope 95 bottles
Distribution CA, FL, OH, TX, WA

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-1049-2020) 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.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. 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?
Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product names, packaged in white plastic bottle with black plastic lid: 1. Aspire Rejuvenation Nutraceuticals, Tranquility PM, Mfg for: Aspire Rejuvenation Nutraceuticals, 74550 Dr Phillips Blvd Ste 205, Orlando, FL 32819. 2. Living Well Clinical Nutrition Center, SleepForce, Manufactured for: living Well Clinical Nutrition, 815 E. Main St Ste A, League City, TX 77573. 3. Swiss Rx Superior Human Performance, Nighttime, Manufactured for Swiss Rx, 1668 Valtec LN STE H, Boulder, CO 80301. 4. energy health, Neuro Calm PM, Mfg for: Energy Health, 709 W. Leuda St., Fort Worth, TX 76104. 5. Nutra Molecular, Nutra Calm PM, Manufactured for: Nutra Molecular, 1543 S Bowen Rd, Pantego, TX 76013. 6. Good Medicine NeuroSleep, Manufactured for: Good Medicine, 5235 Morning Sun Rd, Oxford, OH 45056. 7. WiseMeds Tranquil PM + GABA, Neurotransmitter Support for a Healthy Sleep Cycle. Distributed by: WiseMeds, 534 S. Chickasaw Trail, Orlando, FL 32825. .. Recalled by Provident Nutraceutical div. of Ortho Molecular Products Inc. Units affected: 95 bottles.
Why was this product recalled?
Various branded dietary supplements may contain undeclared soy.
Which agency issued this recall?
This recall was issued by the FDA Food on August 12, 2020. Severity: Moderate. Recall number: F-1049-2020.
Where was the recalled product distributed?
Distribution: CA, FL, OH, TX, WA.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1049-2020) 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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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 August 12, 2020. 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.