Cardinal Health Inc.: Medical Device Recall in 2019 - (Recall #: Z-0702-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Presource Kit Total Joint Pack containing a double-wrapped basin component. Product Usage: This kit is used on patients undergoing joint replacement knee or hip.

Product Classification:

Class II

Date Initiated: November 16, 2018

Date Posted: January 16, 2019

Recall Number: Z-0702-2019

Event ID: 81756

Reason for Recall:

The double wrapping of this custom kit basin set is not supported by the current sterility assurance validation.

Status: Terminated

Product Quantity: 182 packs

Code Information:

Product code: SOP22TJCLK Lot numbers # 104405, 122793, and 987948

Distribution Pattern:

US state of Florida

Voluntary or Mandated:

Voluntary: Firm initiated