Drug recall
BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton…
FDA recall event 66031 · Class II · Becton Dickinson & Company
Key facts
| Event ID | 66031 |
|---|---|
| Recall numbers | Z-2192-2013 |
| Recalling firm | Becton Dickinson & Company |
| Product type | Devices |
| Products | BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and Company, Franklin Lakes, NJ 07417 USA Made in USA. Used to perform heel sticks for… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The Lancet will not retract after activation thus creating a potential for exposure to a used sharp. |
| Initiation date | Jul 10, 2013 |
| Report date | Sep 18, 2013 |
| Termination date | Mar 19, 2014 |
| 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: