Drug recall
Diabetisource AC Advanced-Control Tube Feeding For People With Diabetes. NET 50.7 FL OZ (1500 mL). Not For…
FDA recall event 34023 · Class I · Novartis Nutrition Corp.
Key facts
| Event ID | 34023 |
|---|---|
| Recall numbers | F-112-6 |
| Recalling firm | Novartis Nutrition Corp. |
| Product type | Food |
| Products | Diabetisource AC Advanced-Control Tube Feeding For People With Diabetes. NET 50.7 FL OZ (1500 mL). Not For Parenteral Use. Medical food for use under medical supervision. Novartis Medical Nutrition… |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A portion of RESOURCE Diabetic TF, Lot 2135L, has been incorrectly packaged into containers identified and labeled as Diabetisource AC. RESOURCE Diabetic TF contains caseinate, a component of milk… |
| Initiation date | Nov 11, 2005 |
| City | Saint Louis Park |
| Country | United States |
| FEI number | 2110851 |
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