Becton Dickinson & Company: Medical Device Recall in 2019 - (Recall #: Z-0285-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI: 00801741066023 Power-Trialysis Short-Term Alphacurve Dialysis Catheter with a third internal umen for IV therapy, power injection of contrast media, and central venous pressure monitoring.

Product Classification:

Class II

Date Initiated: September 16, 2019

Date Posted: November 13, 2019

Recall Number: Z-0285-2020

Event ID: 83886

Reason for Recall:

A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.

Status: Terminated

Product Quantity: 75 units

Code Information:

REDR0440

Distribution Pattern:

Distributed to healthcare facilities in AR, FL, IL, NJ, TX, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated