Drug recall
dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only…
FDA recall event 73584 · Class II · Dynarex Corporation
Key facts
| Event ID | 73584 |
|---|---|
| Recall numbers | Z-2057-2016 |
| Recalling firm | Dynarex Corporation |
| Product type | Devices |
| Products | dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product Usage:containers for sample collection |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen containers were packed in incorrect exterior carton. |
| Initiation date | Mar 3, 2016 |
| Report date | Jul 6, 2016 |
| Termination date | Jun 6, 2018 |
| City | Orangeburg |
| State | NY |
| Country | United States |
| FEI number | 2431014 |
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: