PlainRecalls
LowClass IIITerminated

FDA Drug recall · Reported August 27, 2014

Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laboratories, Inc., Sayreville, NJ 08872, NDC 13811-558-30, UPC 3 13811 55830 2.

Labeling: Not Elsewhere Classified: Label indicates that the product contains Vitamin B12 (12 micrograms) on the Supplement Facts panel, however, the formulation of this product d…

Recall #
D-1544-2014
Affected scope
142,732 bottles
Initiated
April 17, 2014
Verify with FDA Drug →
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Trigen Laboratories, Inc. recalled Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laborator… - a low-severity action.

Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laborator… was recalled by Trigen Laboratories, Inc. in August 27, 2014. Reason: Labeling: Not Elsewhere Classified: Label indicates that the product contains Vitamin B12 (12 micrograms) on …. Check the official notice for the remedy. Verify recall #D-1544-2014 with the FDA Drug before acting.

The recall

Trigen Laboratories, Inc. issued this low-severity FDA Drug recall-Labeling: Not Elsewhere Classified: Label indicates that the product contains Vitamin B12 (12 micrograms) on ….

Low
severity level
Class III
classification
August 27, 2014
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-1544-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,014 dietary supplements recalls on record

0100200300400 20072010201320162019202220252026 21
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

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

Product description

Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laboratories, Inc., Sayreville, NJ 08872, NDC 13811-558-30, UPC 3 13811 55830 2.

Reason for recall

Labeling: Not Elsewhere Classified: Label indicates that the product contains Vitamin B12 (12 micrograms) on the Supplement Facts panel, however, the formulation of this product does not contain Vitamin B12.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number D-1544-2014
Date reported August 27, 2014
Date initiated April 17, 2014
Recalling firm Trigen Laboratories, Inc.
Firm location Tampa, FL
Affected scope 142,732 bottles
Distribution Nationwide

Profile values are sourced directly from the official FDA Drug 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 (D-1544-2014) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug 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 Drug 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?
Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laboratories, Inc., Sayreville, NJ 08872, NDC 13811-558-30, UPC 3 13811 55830 2.. Recalled by Trigen Laboratories, Inc.. Units affected: 142,732 bottles.
Why was this product recalled?
Labeling: Not Elsewhere Classified: Label indicates that the product contains Vitamin B12 (12 micrograms) on the Supplement Facts panel, however, the formulation of this product does not contain Vitamin B12.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 27, 2014. Severity: Low. Recall number: D-1544-2014.
Where was the recalled product distributed?
Distribution: Nationwide.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Goody King Magnetic Building Cubes and Blocks Recalled Due … → · All Dietary Supplements recalls

This recall: FDA Drug, reported August 27, 2014. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026