Drug recall
Aziffa Capsules Dietary Supplement, sold in bulk, Novacare, LLC, Midvale, UT
FDA recall event 56562 · Class I · Novacare, LLC
Key facts
| Event ID | 56562 |
|---|---|
| Recall numbers | D-168-2011, D-169-2011, D-170-2011, D-171-2011, D-172-2011, D-173-2011, D-174-2011, D-175-2011, D-176-2011, D-177-2011, D-178-2011, D-179-2011 and 9 more |
| Recalling firm | Novacare, LLC |
| Product type | Drugs |
| Products | Aziffa Capsules Dietary Supplement, sold in bulk, Novacare, LLC, Midvale, UT, Erex Capsules Dietary Supplement, sold in bulk, Novacare, LLC, Midvale, UT, Eyeful Capsules Dietary Supplement, sold in bulk, Novacare, LLC, Midvale, UT, Hard Drive Capsules Dietary Supplement, sold in bulk, Novacare, LLC, Midvale, UT, Libidinal Capsules Dietary Supplement, packaged in 15ct bottles and 30ct bottles, Novacare, LLC, Midvale, UT and 16 more |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Marketed Without an Approved NDA/ANDA; product contains sulfoaildenafil, an analogue of sildenafil, the active ingredient used in an FDA approved product for the treatment of male erectile…, Marketed Without an Approved NDA/ANDA; product may contain sulfoaildenafil, an analogue of sildenafil, the active ingredient in an FDA approved product used for the treatment of male erectile…, Marketed… |
| Initiation date | Aug 9, 2010 |
| Termination date | Jan 18, 2013 |
| City | Salt Lake City |
| State | UT |
| Country | United States |
| FEI number | 1000220648 |
At a glance
- 10–99 Products in this recall
- None 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