Drug recall
Blanketrol III Data Export Software Version 1.10 The Blanketrol III Data Export Software is intended for use…
FDA recall event 66632 · Class II · Cincinnati Sub-Zero Products Inc
Key facts
| Event ID | 66632 |
|---|---|
| Recall numbers | Z-0443-2014 |
| Recalling firm | Cincinnati Sub-Zero Products Inc |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | May 15, 2013 |
| Report date | Dec 11, 2013 |
| Termination date | May 13, 2014 |
| City | Cincinnati |
| State | OH |
| Country | United States |
| FEI number | 1516825 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: