Becton Dickinson & Company: Medical Device Recall in 2016 - (Recall #: Z-0740-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perform the spinal anesthesia procedure

Product Classification:

Class II

Date Initiated: November 7, 2016

Date Posted: December 21, 2016

Recall Number: Z-0740-2017

Event ID: 75802

Reason for Recall:

BD is conducting a voluntary product recall of the BD Spinal Anesthesia Tray, Cat (Ref) 405671, lot B01K089D since a very low number of trays are incorrectly labeled as BD Single Shot Epidural Tray, Cat (Ref) 406069.

Status: Terminated

Product Quantity: 4500

Code Information:

B01K089D

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated