Class II — Kimberly-Clark Corporation
| Recalling firm | KIMBERLY-CLARK CORPORATION |
|---|---|
| Registered facility | KIMBERLY-CLARK PERU S.R.L. - Santa Clara Mill (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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 |
| Quantity | 389,300 units |
| Distribution | U.S. Nationwide Distribution |
| Initiated | 2013-10-24 |
| Classified | 2013-12-16 |
| Terminated | 2017-08-25 |
| Recall number | Z-0518-2014 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Kimberly-Clark Corporation (Z-0518-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/66859/
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