Carefusion 2200 Inc: Medical Device Recall in 2018 - (Recall #: Z-1425-2018)

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:

JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 3.5, d.) 8G x 6, e.) 11G x 6]; STERILE;

Product Classification:

Class II

Date Initiated: February 23, 2017

Date Posted: April 25, 2018

Recall Number: Z-1425-2018

Event ID: 76620

Reason for Recall:

The integrity of the sterile packaging is potentially compromised.

Status: Terminated

Product Quantity: 14,200 units

Code Information:

Product Code: a.) TJM3513 / LOT 0000836582, 0000838949, 0000843968, 0000849685, 0000852933; b.) TJM4008 / LOT 0000841349, 0000841348, 0000843961, 0000849132, 0000852123, 0000853877; c.) TJM4011 / LOT 0000836575, 0000838950, 0000840195, 0000843075, 0000843076, 0000846708, 0000852932, 0000853878, 0000854861, 0000854983; d.) TJM6008 / LOT 0000842725, 0000853971; e.) TJM6011 / LOT 0000843077, 0000849713, 0000854659

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