Drug recall
Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100…
FDA recall event 70128 · Class II · Baxter Corporation Englewood
Key facts
| Event ID | 70128 |
|---|---|
| Recall numbers | Z-1227-2015 |
| Recalling firm | Baxter Corporation Englewood |
| Product type | Devices |
| Products | Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels. |
| Initiation date | Dec 29, 2014 |
| Report date | Mar 11, 2015 |
| Termination date | Aug 8, 2016 |
| 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: