Severity
Moderate
FDA Food recall · Reported August 19, 2015
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
Novacare, LLC recalled Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily w… - a moderate-severity action.
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily w… was recalled by Novacare, LLC in August 19, 2015. Reason: TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.. Check the official notice for the remedy. Verify recall #F-2946-2015 with the FDA Food before acting.
The recall
Novacare, LLC issued this moderate-severity FDA Food recall-TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling..
Sourced from official FDA Food enforcement records. Verify recall #F-2946-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-2946-2015) was formally reported on August 19, 2015, with the manufacturer initiating the action on May 27, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. Novacare, LLC is listed as the recalling firm, operating out of Murray, UT. Federal records list the affected scope as 961 bottles..
The documented reason for this recall is: TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling. Distribution data in the federal record shows the product reached: Nationwide. No foreign or VA/govt/military consignees.. 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.
Where this recall sits in its category - 14,287 drugs & medications 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 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
961 bottles.
Related Recalls
6
1 from same agency
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2946-2015 |
| Date reported | August 19, 2015 |
| Date initiated | May 27, 2015 |
| Recalling firm | Novacare, LLC |
| Firm location | Murray, UT |
| Affected scope | 961 bottles. |
| Distribution | Nationwide. No foreign or VA/govt/military consignees. |
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.
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.
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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 19, 2015. 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.