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On October 19, 2004, she was kidnapped by an unidentified Islamist militant group in Baghdad, who recorded her execution in a hostage video two weeks after her kidnapping. Her remains have never been recovered, and her killer, architect Ali Lutfi Jassar al-Rawi, escaped from prison in 2010, with his whereabouts still unclear.
The file cross-references unidentified bodies against records in the Missing Persons File. U.S. Secret Service Protective File: Records containing names and other information on people who are believed to pose a threat to the U.S. president and/or others afforded protection by the U.S. Secret Service .
Per a 2017 report, the U.S. states of Oregon, Arizona, and Alaska have the highest numbers of missing-person cases per 100,000 people. [6] In Canada—with a population a little more than one tenth that of the United States—the number of missing-person cases is smaller, but the rate per capita is higher, with an estimated 71,000 reported in ...
The U.S. Drug Enforcement Administration is also seeking information on two others. ... Mexico cartel crime had escalated with more than 40,000 cases of 26,000 unidentified bodies in morgues and ...
This is a list of government-sponsored investigations or reports related to UFOs. Brazil ... and Investigation of Complaints of Unidentified Flying ...
In February 1981, a composite sketch and tips led to his arrest. Evidence linked him to at least 12 murders and numerous assaults. Convicted in 1981, Woodfield received a life sentence plus 165 years.
Martha Marie Morrison (1956 – September 1974) was a 17-year-old American girl who was murdered in 1974, and whose remains went unidentified for over 40 years after their discovery. Morrison, a resident of Portland, Oregon , disappeared under mysterious circumstances in September 1974.
First, there is no certainty that the reported event was actually due to the product. The FDA does not require that a causal relationship between a product and event be proven, and reports do not always contain enough detail to properly evaluate an event. Further, the FDA does not receive all adverse event reports that occur with a product.