Carefusion 2200 Inc: Medical Device Recall in 2018 - (Recall #: Z-1421-2018)

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:

Manometer, 550 ml three-Way Stopcock; STERILE;

Product Classification:

Class II

Date Initiated: February 23, 2017

Date Posted: April 25, 2018

Recall Number: Z-1421-2018

Event ID: 76620

Reason for Recall:

The integrity of the sterile packaging is potentially compromised.

Status: Terminated

Product Quantity: 4,240 units

Code Information:

Product Code: 4330 Lot Code: 0000837810; 0000840335; 0000842213; 0000848531; 0000851181; 0000853962

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