Drug recall
Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198)…
FDA recall event 66859 · Class II · Kimberly-Clark Corporation
Key facts
| Event ID | 66859 |
|---|---|
| Recall numbers | Z-0518-2014 |
| Recalling firm | Kimberly-Clark Corporation |
| Product type | Devices |
| Products | Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7 mL Epilor plastic Luer-Lok LOR Syringes under recall by Becton Dickinson (BD) because the product may stall or stick when… |
| Initiation date | Oct 24, 2013 |
| Report date | Dec 25, 2013 |
| Termination date | Aug 25, 2017 |
| City | Roswell |
| State | GA |
| Country | United States |
| FEI number | 1000015879 |
At a glance
- 1–9 Products in this recall
- 1–9 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: