Drug recall
BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a…
FDA recall event 89486 · Class III · Becton Dickinson & Company
Key facts
| Event ID | 89486 |
|---|---|
| Recall numbers | Z-0665-2022 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a catheter port equipped with a threaded female luer during blood or urine sample… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000 Analyzers and lead to false elevations… |
| Initiation date | Jan 6, 2022 |
| Report date | Mar 2, 2022 |
| City | Franklin Lakes |
| State | NJ |
| Country | United States |
| FEI number | 2243072 |
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: