Drug recall
Triveen - PRx RNF Capsules, 30-count bottles, Rx only; Manufactured for: Trigen Laboratories, Inc…
FDA recall event 68685 · Class III · Trigen Laboratories, Inc.
Key facts
| Event ID | 68685 |
|---|---|
| Recall numbers | D-1544-2014 |
| Recalling firm | Trigen Laboratories, Inc. |
| Product type | Drugs |
| Products | 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. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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… |
| Initiation date | Apr 17, 2014 |
| Report date | Aug 27, 2014 |
| Termination date | Jul 26, 2017 |
| City | Tampa |
| State | FL |
| Country | United States |
| FEI number | 3009428989 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: