v.1.2 Upgrade Kit or v.1.2 upgrade installed on recall: Software Issue
v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System, Model H700123. The WorkMate Claris" System is a computer-based…
Why was v.1.2 Upgrade Kit or v.1.2 upgrade installed on recalled?
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial Numbers: 14399319, 15508962, 18782712, 18855856
- Product
- v.1.2 Upgrade Kit or v.1.2 upgrade installed on WorkMate Claris System, Model H700123. The WorkMate Claris" System is a computer-based…
- Recalling firm
- Abbott Laboratories Inc. (St Jude Medical)
- Quantity
- 4 units
- Distribution
- US Nationwide distribution in the states of MI, KS, MO, TX.
- Recall date
- June 23, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)