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Terminated

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

FDA Recall Z-0518-2014 · Posted 2013-12-16

Recalling FirmKimberly-Clark Corporation
Recall StatusTerminated
Product CodeCAZ
Date Initiated2013-10-24
Date Terminated2017-08-25
Product Quantity389,300 units

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 traveling within the barrel of the syringe.

Firm Action

Kimberly Clark Corporation sent a Product Advisory Notice letter to affected consignees. The letter identified the affected product, problem and actions to be taken. For questions call 770-587-8393 or via email

Root Cause

Component design/selection

Distribution Pattern

U.S. Nationwide Distribution

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K941153EPI-SPINAL ANESTHESIA TRAYPreferred Medical Products · 1995-05-30

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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