Loading...
Loading...
All product recalls associated with Becton Dickinson Infusion Therapy Systems, Inc..
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Due to a manufacturing defect IV catheter may have a hole in the septum, which may result in blood leakage from the septum during insertion, which may cause blood exposure or the need for a second IV to be placed - which may result in therapy delay.
Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.