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Kimberly-Clark Corporation recalls Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usag
Recalled December 25, 2013 · FDA recall Z-0518-2014 · Kimberly-Clark
Hazard
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 traveling within the barrel of the syringe. · FDA Class II
Units
389,300 units
Sold at
U.S. Nationwide Distribution
Description
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 traveling within the barrel of the syringe.
Product
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 syringes, needles and drugs
Manufacturer(s)
Kimberly-Clark Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →