Carefusion 2200 Inc: Medical Device Recall in 2018 - (Recall #: Z-1422-2018)

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 NEEDLE BIOPSY [15G X 100MM DISP, 16G X 100MM DISP, 17G X 100MM, 16G X 70MM DISP]; STERILE;

Product Classification:

Class II

Date Initiated: February 23, 2017

Date Posted: April 25, 2018

Recall Number: Z-1422-2018

Event ID: 76620

Reason for Recall:

The integrity of the sterile packaging is potentially compromised.

Status: Terminated

Product Quantity: 790 units

Code Information:

Product Code: SN1015X / LOT 0000840334 ; Product Code: SN1016X / LOT 0000848028 ; Product Code: SN1017X / LOT 0000848018 ; Product Code SN7016X / LOT 0000848017

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