FDA Drug recall D-1544-2014
Triveen - PRx RNF Capsules, 30-count bottles, Rx only
- FDA Drug
- Class III
- terminated
- Published 2014-08-27
On 2014-08-27 the FDA classified a Class III recall of Triveen - PRx RNF Capsules, 30-count bottles, Rx only by Trigen Laboratories, citing 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….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1544-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-04-17 |
| Published | 2014-08-27 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Trigen Laboratories |
| Distribution | US |
Product
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
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.
Identifiers
| upc | 313811558302 |
|---|---|
| code_info | Lot #: 505024006, 505024007, Exp 03/15; 505024008; 505024009, Exp 06/15; 505024010, Exp 08/15; 505024011, Exp 09/15; and 505024012, Exp 10/15 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1544-2014%22
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