Drug recall
Conray 43 (Iothalamate meglumine Injection USP 43%), 202 mg/mL Organically Bound Iodine, 100mL bottle, Rx…
FDA recall event 25448 · Class III · Tyco Healthcare
Key facts
| Event ID | 25448 |
|---|---|
| Recall numbers | D-176-3 |
| Recalling firm | Tyco Healthcare |
| Product type | Drugs |
| Products | Conray 43 (Iothalamate meglumine Injection USP 43%), 202 mg/mL Organically Bound Iodine, 100mL bottle, Rx only, For Intravascular Use, Sterile Solution, Mallinckrodt Inc., St Louis, MO 63042 NDC… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Misbranding; product has no immediate bottle label |
| Initiation date | Jun 25, 2001 |
| City | Raleigh |
| Country | United States |
| FEI number | 3003495779 |
At a glance
- 1–9 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