Reported Jun 23, 2021 · Terminated

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

Abbott Laboratories Inc. (St Jude Medical)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Abbott Laboratories Inc. (St Jude Medical) · 1 Saint Jude Medical Dr · Saint Paul, MN · 55117-1789

Is this the product you have?

    • WorkMate Claris v.1.2 Upgrade Kits
    • Model Numbers H800007 and H800012
Lot codes and dates
  • None
Amount recalled
8 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 18, 2024 · Data as of Sep 19, 6:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.