BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.
Recall
- Recall Number
- Z-1317-2015
- Event Number
- 70593
- Firm
- Becton Dickinson & Company
- FEI Number
- 2243072
- Product Code
- FPA
- Status
- Terminated
- Root Cause
- Process control
- Initiated
- February 19, 2015
- Posted
- March 25, 2015
- Terminated
- May 25, 2017
- Address
- 1 Becton Dr, Franklin Lakes, NJ, 07417-1815
Description
BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.
Becton Dickinson received an elevated number of complaints for blood or infusate/medication leakage due to tearing of the silicone septum.
Becton Dickinson sent an Urgent Voluntary Product Recall Letter/Recall Response Card/Packing Instructions, dated 2/19/15, to their affected customers via UPS next day mail. The letters identified the affected device and explained the reason for the recall. Customers were to review their inventory for the specific catalog and lot numbers provided and quarantine the affected product. The Recall Response Card form should be completed and faxed back to BD at 1-866-514-2113 or e-mail [email protected]. All affected product should be returned with the completed Recall Response Card following the steps on the enclosed packing instruction. Upon receipt of the returned product, BD will send customers replacement product. If customers have questions or require assistance, they should contact 1-866-800-2917.
Distributed to the states of CA, CT, FL, IL, MA, ND, NY, OH and PA.
315,800 units