Halyard Health: Medical Device Recall in 2015 - (Recall #: Z-1222-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

KimVent Wet Pak, Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.

Product Classification:

Class II

Date Initiated: January 16, 2015

Date Posted: March 11, 2015

Recall Number: Z-1222-2015

Event ID: 70397

Reason for Recall:

Defect: A hole or crack was found which may cause air to leak.

Status: Terminated

Product Quantity: 83 cases (20 tubes per case)

Code Information:

Product Code; 22108147, Wet Pak Lot number: AB4195U14, AB4216U06 & AB4230U16, KimVent Lot Number: M4132T643.

Distribution Pattern:

CA, FL, IL, LA, MA, MK, MN, MS, NM, NY, OK and TX and Japan.

Voluntary or Mandated:

Voluntary: Firm initiated