Drug recall
Chromagen Caplet, Rx, an oral iron supplement packaged in 90 caplet bottles. Marketed by Ther-Rx Corporation…
FDA recall event 51092 · Class II, Class III · Ther-Rx Corp
Key facts
| Event ID | 51092 |
|---|---|
| Recall numbers | D-238-2009, D-239-2009, D-240-2009, D-241-2009, D-242-2009, D-243-2009, D-244-2009, D-245-2009, D-246-2009, D-247-2009, D-248-2009, D-249-2009 and 7 more |
| Recalling firm | Ther-Rx Corp |
| Product type | Drugs |
| Products | Chromagen Caplet, Rx, an oral iron supplement packaged in 90 caplet bottles. Marketed by Ther-Rx Corporation, St. Louis, MO. NDC 64011-198-26, Chromagen FA caplet, , Rx. an oral iron supplement packaged in 90 caplet bottles. Marketed by Ther-Rx Corporation, St. Louis, MO, NDC 64011-199-26, Chromagen Forte caplet, Rx, an oral iron supplement packaged in 90 caplet bottles, Marketed by Ther-Rx Corporation, St. Louis, MO, NDC 64011-197-26, Encora capsule/tablet, each carton contains 30 capsules and 30 tablets packaged in individual blisters, NDC 64011-166-36, Rx. Marketed by Ther-Rx Corporation, St. Louis, MO., Niferex 150 Forte Capsule, Rx, packaged in 90 capsule bottles. Marketed by Ther-Rx Corporation, St. Louis, MO, NDC 64011-164-26 and 14 more |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The products were not manufactured in conformance with GMP's |
| Initiation date | Jan 28, 2009 |
| Termination date | Apr 2, 2012 |
| City | Bridgeton |
| State | MO |
| Country | United States |
| FEI number | 3006094186 |
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