Drug recall
1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog…
FDA recall event 73691 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 73691 |
|---|---|
| Recall numbers | Z-1690-2016 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog number 381700 2) 24 G x 0.56 in. BD Angiocath-N" Autoguard" shielded IV catheter (0.7 mm x… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage. |
| Initiation date | Mar 18, 2016 |
| Report date | May 25, 2016 |
| Termination date | Jul 19, 2017 |
| City | Franklin Lakes |
| State | NJ |
| Country | United States |
| FEI number | 2243072 |
At a glance
- 1–9 Products in this recall
- 10–99 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: