Drug recall
BARD¿ BrachySource¿ Iodine125 radioactive seeds consist of a welded titanium capsule containing the I125…
FDA recall event 79972 · Class II · Bard Brachytherapy, Inc.
Key facts
| Event ID | 79972 |
|---|---|
| Recall numbers | Z-1702-2018 |
| Recalling firm | Bard Brachytherapy, Inc. |
| Product type | Devices |
| Products | BARD¿ BrachySource¿ Iodine125 radioactive seeds consist of a welded titanium capsule containing the I125 absorbed onto a nickel / copper-coated, gold-cored aluminum wire (reference Figure 1 below)… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Bard Medical Division is recalling the BARD¿ BrachySource¿ Iodine125 Radioactive Seeds in Mick¿ Applicators and BARD¿ BrachySource¿ Iodine125 Radioactive Seeds Loose in Vial with Sterile Spacers… |
| Initiation date | Apr 10, 2018 |
| Report date | May 16, 2018 |
| Termination date | Jun 5, 2020 |
| City | Carol Stream |
| State | IL |
| Country | United States |
| FEI number | 3002942387 |
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: