Carefusion 2200 Inc: Medical Device Recall in 2018 - (Recall #: Z-1423-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;

Product Classification:

Class II

Date Initiated: February 23, 2017

Date Posted: April 25, 2018

Recall Number: Z-1423-2018

Event ID: 76620

Reason for Recall:

The integrity of the sterile packaging is potentially compromised.

Status: Terminated

Product Quantity: a.) 13,010 units b.) 2116 units

Code Information:

Product Code: a.) TIN3015/ LOT 0000836578, 0000841213, 0000841215, 0000842719, 0000842721, 0000845423, 0000848061, 0000849715, 0000850938, 0000852076, 0000854859; Product Code: b.) TIN3018/ LOT 0000836574, 0000841212, 0000852078

Distribution Pattern:

Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated