Kimberly-Clark Corporation Kimberly Clark * 20' Minibore Extension Line * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA. This is a Pain Management Product that is sold in a wide variety of kits including both standard tray configurations and custom kits. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Kimberly Clark * 20' Minibore Extension Line * Single Use * Sterile * Rx only * Manufactured by Ballard Medical Products, Draper, Utah, 84020 USA * Distributed in the U.S. by Kimberly Clark Global States, Inc., Roswell, GA 30076, USA. This is a Pain Management Product that is sold in a wide variety of kits including both standard tray configurations and custom kits.
Brand
Kimberly-Clark Corporation
Lot Codes / Batch Numbers
Product Code: 18938, Lot #321922
Products Sold
Product Code: 18938, Lot #321922
Kimberly-Clark Corporation is recalling Kimberly Clark * 20' Minibore Extension Line * Single Use * Sterile * Rx only * Manufactured by Ball due to There exists a possibility that the Pain Management Procedural Trays may contain extension sets that do not meet USP specification requirements for no. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There exists a possibility that the Pain Management Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).
Recommended Action
Per FDA guidance
Consignees were notified via fax on/about 03/15/2006.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026