Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD Recalled by Kimberly-Clark Corporation Due to Kimberly-Clark Single Shot Epidural Pain Management Trays contain...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Kimberly-Clark Corporation directly.
Affected 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 syringes, needles and drugs
Quantity: 389,300 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Kimberly-Clark Corporation
Kimberly-Clark Corporation has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report