ON-SITE SCREENING, INC. & Ronald L. Lealos, Plaintiffs-Appellants, v. UNITED STATES of America, Defendant-Appellee.
No. 11-2895.
United States Court of Appeals, Seventh Circuit.
Argued May 22, 2012. Decided July 25, 2012.
690 F.3d 896
Donald R. Lorenzen (argued), Office of the United States Attorney, Chicago, IL, for Defendant-Appellee.
Before EASTERBROOK, Chief Judge, and WILLIAMS and TINDER, Circuit Judges.
TINDER, Circuit Judge.
Ronald Lealos, through his company On-Site Screening, Inc. (On-Site), sought to develop a rapid, self-administered test to determine a person‘s HIV status. The development process included the collection of human blood and saliva samples. On-Site sued the United States under the Federal Tort Claims Act (FTCA) for the destruction of its blood and saliva specimens by the Food and Drug Administra-
I. Factual Background
We review the grant of summary judgment de novo construing all relevant facts in the appellants’ favor. MMG Fin. Corp. v. Midwest Amusements Park, LLC, 630 F.3d 651, 656 (7th Cir. 2011). On-Site must point to facts showing a genuine issue for trial to win reversal. Id. Normally we review a district court‘s enforcement of its local rules for an abuse of discretion, Patterson v. Ind. Newspapers, Inc., 589 F.3d 357, 360 (7th Cir. 2009), but the appellants do not contest the finding that they failed to follow local rules.
The government‘s investigation of On-Site started in October 2004 when a local fire inspector informed the FDA that materials labeled HIV-positive were in a Bedford Park laboratory that made over-the-counter products like shampoos and deodorants. Jocelyn Ellis, a special agent in the FDA‘s office of criminal investigations, began investigating. After receiving written consent from the facility‘s owner, she found and removed blood and saliva specimens labeled HIV-positive from a refrigerator at the facility. Ellis deemed the specimens evidence in her investigation and placed them in storage in an Illinois Department of Public Health laboratory freezer. Ellis closed her investigation about four years later with the U.S. Attorney‘s Office declining to prosecute On-Site or its owner appellant Ronald Lealos and the FDA‘s Chicago district office declining to pursue a civil regulatory action. With Ellis‘s investigation over, the FDA contacted Lealos to see whether he wanted On-Site‘s specimens returned or destroyed. Lealos said he wanted the specimens back. Yet sometime before this the freezer in which the specimens were stored stopped operating causing the destruction of the blood and saliva specimens.
On-Site sued the United States under the FTCA alleging bailment, negligence, and breach of internal agency rules and protocols requiring the agency to maintain evidence in the condition in which it was discovered. The United States moved to dismiss on grounds that an exception to the FTCA‘s waiver of sovereign immunity—
II. Analysis
The FTCA waives the government‘s sovereign immunity for money damages claims for the loss of property caused by negligent or wrongful acts or omissions of government employees acting within the scope of their office or employment in circumstances where a private person would be liable.
On-Site argues we should use an agency publication discussing seizures and detentions to determine whether the government seized its specimens. See U.S. Food and Drug Administration, Inspections, Compliance, Enforcement, and Criminal Investigations, 2.7 Detention Activities, www.fda.gov/ICECI/Inspections/IOM/ucm122515.htm#SUB2.7 (last visited July 20, 2012); U.S. Food and Drug Administration, Inspections, Compliance, Enforcement, and Criminal Investigations, 6-1 Seizure, www.fda.gov/ICECI/ComplianceManuals/RegulatoryProceduresManual/ucm176733.htm (last visited July 20, 2012). On-Site maintains that this publication characterizes the FDA actions as a seizure within the
Despite what an agency publication may say, for purposes of interpreting this federal statute, the “ordinary meaning of the words used” governs what constitutes a detention by a law enforcement officer. See Kosak v. United States, 465 U.S. 848, 853, 104 S. Ct. 1519, 79 L. Ed. 2d 860 (1984) (quoting Am. Tobacco Co. v. Patterson, 456 U.S. 63, 68, 102 S. Ct. 1534, 71 L. Ed. 2d 748 (1982)). And “the fairest interpretation” of “‘any claim arising in respect of the detention of goods ... includes a claim resulting from negligent handling or storage of detained property.‘” Id. at 854, 104 S. Ct. 1519 (quoting
On-Site fails to point to any evidence showing that there is a genuine dispute
On-Site also argues that we should preclude the government from asserting sovereign immunity as a defense to this litigation because it did not base its denial of On-Site‘s administrative claim on that doctrine or claim that a law enforcement official detained the specimens.2 But ex-
On-Site also fails to show that the district court abused its discretion in denying its request to amend because doing so would be futile. See Johnson v. Cypress Hill, 641 F.3d 867, 872 (7th Cir. 2011) (district courts have broad discretion to deny leave to amend “where the amendment would be futile“). On-Site‘s amended complaint sought compensation from the United States under the FTCA for the destruction of the specimens Ellis took from the Bedford Park laboratory. However characterized, the tort claims raised in the proposed amended complaint fall within the FTCA‘s preservation of sovereign immunity for claims involving law enforcement officers detaining property, see
Finally, almost as an aside, On-Site also asks that we declare that it is entitled to a Tucker Act remedy or order the district court not to disturb any potential Tucker remedy it might have. See
III. Conclusion
We AFFIRM the district court‘s judgment dismissing On-Site‘s complaint with prejudice.
