Overview of recall records associated with Becton, Dickinson and Company, including dates, categories and classifications where available.
Classification mix: Class II: 108, Class I: 16, Class III: 1.
The products have been confirmed to have reduced or no additive within the tube reservoir. The tubes may develop visible clots within the tube samples or micro clots that are not easily…
An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the potential to lead to…
Leaking of the Smartsite Syringe Administration Set. May result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to infusates.
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
The luer could break and cause the device to leak or break off and get stuck in the fistula needle port rendering the port inaccessible for dialysis. As a result, the patient would need to…
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical…
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical…
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical…
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends following Good Clinical…
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
One lot of the specified needles is not performing as intended due to a failure in the needle tip shield/safety mechanism, which may lead to an increased risk of a contaminated needlestick…
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection Tubes (2.7mL) (light blue top tube) will exhibit over fill draw volumes from ~11-14%.
Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection Tubes (2.7mL) (light blue top tube) will exhibit over fill draw volumes from ~11-14%.
Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection Tubes (2.7mL) (light blue top tube) will exhibit over fill draw volumes from ~11-14%.
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
Increased amount of residual blood present on the top of stopper well after venipuncture
BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer Lithium Heparin Green Top Tubes can cause an underestimation of lead in blood samples when used with Magellan…
This page summarizes recall records in which the official source identifies Becton, Dickinson and Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
