Drug recall
Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes
FDA recall event 72086 · Class II · Arrow International Inc
Key facts
| Event ID | 72086 |
|---|---|
| Recall numbers | Z-2825-2015 |
| Recalling firm | Arrow International Inc |
| Product type | Devices |
| Products | Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to compromised sterility of the outer barrel, Arrow purchased recalled items that were packaged with certain products. |
| Initiation date | Aug 27, 2015 |
| Report date | Oct 7, 2015 |
| Termination date | Jun 18, 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: