Drug recall
RAPIDFILL Syringe Strip, For use with RAPIDFILL Automated Syringe Filler (ASF): H93890200 RAPIDFILL Syringe…
FDA recall event 68030 · Class II · Baxter Corporation Englewood
Key facts
| Event ID | 68030 |
|---|---|
| Recall numbers | Z-1620-2014 |
| Recalling firm | Baxter Corporation Englewood |
| Product type | Devices |
| Products | RAPIDFILL Syringe Strip, For use with RAPIDFILL Automated Syringe Filler (ASF): H93890200 RAPIDFILL Syringe Strip, White. H93890221 RAPIDFILL Syringe Strip, Yellow. H93890222 RAPIDFILL Syringe Strip… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Possible breach in sterile barrier for inner and outer bags of the product. |
| Initiation date | Apr 16, 2014 |
| Report date | May 21, 2014 |
| Termination date | Mar 23, 2015 |
| City | Englewood |
| State | CO |
| Country | United States |
| FEI number | 1419106 |
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: