Drug recall
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in…
FDA recall event 68989 · Class II · Centurion Medical Products Corporation
Key facts
| Event ID | 68989 |
|---|---|
| Recall numbers | Z-2670-2014 |
| Recalling firm | Centurion Medical Products Corporation |
| Product type | Devices |
| Products | 0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion Convenience Kits. Recalled product is attached to the outside of the Convenience Kits. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Unit packages may exhibit open seals which impacts package integrity and potentially product sterility. |
| Initiation date | Jul 25, 2014 |
| Report date | Oct 1, 2014 |
| Termination date | Nov 25, 2014 |
| City | Williamston |
| State | MI |
| Country | United States |
| FEI number | 3008403546 |
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: