Abbott Laboratories Inc. (St Jude Medical): Medical Device Recall in 2021 - (Recall #: Z-1855-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012

Product Classification:

Class II

Date Initiated: May 5, 2021

Date Posted: June 23, 2021

Recall Number: Z-1855-2021

Event ID: 87904

Reason for Recall:

Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.

Status: Terminated

Product Quantity: 8 units

Code Information:

None

Distribution Pattern:

US Nationwide distribution in the states of MI, KS, MO, TX.

Voluntary or Mandated:

Voluntary: Firm initiated