Becton Dickinson & Company: Medical Device Recall in 2013 - (Recall #: Z-1923-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access devices such as needles, blood collection sets, ad infusion sets to blood collection tubes.

Product Classification:

Class II

Date Initiated: May 1, 2013

Date Posted: August 14, 2013

Recall Number: Z-1923-2013

Event ID: 65322

Reason for Recall:

BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume.

Status: Terminated

Product Quantity: 37,906,400 units

Code Information:

Marketing Status: Class II, 510K # K991088 Device Listing Number: D030347 Catalog number 367290, 367300 (CE), 368491, and 303380.

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated