WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012
Reported: June 23, 2021 Initiated: May 5, 2021 #Z-1855-2021
Product Description
WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012
Reason for Recall
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
Details
- Recalling Firm
- Abbott Laboratories Inc. (St Jude Medical)
- Units Affected
- 8 units
- Distribution
- US Nationwide distribution in the states of MI, KS, MO, TX.
- Location
- Saint Paul, MN
Frequently Asked Questions
What product was recalled? ▼
WorkMate Claris v.1.2 Upgrade Kits, Model Numbers H800007 and H800012. Recalled by Abbott Laboratories Inc. (St Jude Medical). Units affected: 8 units.
Why was this product recalled? ▼
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 23, 2021. Severity: Moderate. Recall number: Z-1855-2021.
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