Deltec, Inc Ventra Percutaneous Intravenous Catheter Repair Kit for Luer Connector Segments and Single-Lumen Catheters, Reorder Number 21-0105 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ventra Percutaneous Intravenous Catheter Repair Kit for Luer Connector Segments and Single-Lumen Catheters, Reorder Number 21-0105
Brand
Deltec, Inc
Lot Codes / Batch Numbers
Lot numbers M20689, 90299, 85047
Products Sold
Lot numbers M20689, 90299, 85047
Deltec, Inc is recalling Ventra Percutaneous Intravenous Catheter Repair Kit for Luer Connector Segments and Single-Lumen Cat due to Silicone adhesive in kits used to repair damaged catheters did not set (cure) properly and remained in a tacky state.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Silicone adhesive in kits used to repair damaged catheters did not set (cure) properly and remained in a tacky state.
Recommended Action
Per FDA guidance
A recall letter, sent to the consignees on July 8, 2003, gave them the option of returning the kits or waiting for the firm to provide them with replacement silicone adhesive.
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 noticeDistribution
As reported by FDA
CA, IL, IN, KS, MI, MN, MO, PA, TX
Page updated: Jan 10, 2026