Drug recall
The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein.
FDA recall event 76637 · Class II · Arrow International Inc
Key facts
| Event ID | 76637 |
|---|---|
| Recall numbers | Z-1705-2017 |
| Recalling firm | Arrow International Inc |
| Product type | Devices |
| Products | The CG+ Arrow PIC Catheters permit venous access to the central circulation through a peripheral vein. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Arrow International, Inc. notified its customers who received the affected Antimicrobial/Antithrombogenic PICC Kits, that the kits were being recalled due to a labeling error. The lidstock on some of… |
| Initiation date | Mar 3, 2017 |
| Report date | Apr 12, 2017 |
| Termination date | Feb 27, 2018 |
| City | Reading |
| State | PA |
| Country | United States |
| FEI number | 2518433 |
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: