Recall Z-0443-2014— Cincinnati Sub-Zero Products Inc
Class II · Terminated
Class II FDA medical device recall by Cincinnati Sub-Zero Products Inc, initiated 2013-05-15, terminated 2014-05-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Blanketrol III Data Export Software Version 1.10 The Blanketrol III Data Export Software is intended for use in the electronic transfer of medical device data from the Blanketrol III to a computer, without controlling or altering the function or parameters of the Blanketrol III.. Reason: During a customer inquiry regarding a beta version of the Bill Data Export Software, Model USB-127, it was discovered that the wrong software version was released to a customer..
- Recalling firm
- Cincinnati Sub-Zero Products Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-05-15
- Terminated
- 2014-05-13
- Firm location
- Cincinnati, OH, United States
Product description
Blanketrol III Data Export Software Version 1.10 The Blanketrol III Data Export Software is intended for use in the electronic transfer of medical device data from the Blanketrol III to a computer, without controlling or altering the function or parameters of the Blanketrol III.
Reason for recall
During a customer inquiry regarding a beta version of the Bill Data Export Software, Model USB-127, it was discovered that the wrong software version was released to a customer.
Data sourced from openFDA. This site is unofficial and independent of the FDA.