FEDERAL · 42 U.S.C. · Chapter 6A

Liability regarding emergency use of automated external defibrillators

Current through Pub. L. 119-102
Title 42The Public Health and Welfare·Ch. 6A — PUBLIC HEALTH SERVICE·Subch. I·Pt. B
(a)Good Samaritan protections regarding AEDs Except as provided in subsection (b), any person who uses or attempts to use an automated external defibrillator device on a victim of a perceived medical emergency is immune from civil liability for any harm resulting from the use or attempted use of such device; and in addition, any person who acquired the device is immune from such liability, if the harm was not due to the failure of such acquirer of the device—
(1)to notify local emergency response personnel or other appropriate entities of the most recent placement of the device within a reasonable period of time after the device was placed;
(2)to properly maintain and test the device; or
(3)to provide appropriate training in the use of the device to an employee or agent of the acquirer

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42 U.S.C. § 238q (Liability regarding emergency use of automated external defibrillators) — published by Counsel Stack Legal Research, free access to 12M+ legal documents.

Related

§ 233
42 U.S.C. § 233
§ 1346
42 U.S.C. § 1346
§ 301
21 U.S.C. § 301

Source Credit

History

(July 1, 1944, ch. 373, title II, §248, as added Pub. L. 106–505, title IV, §404, Nov. 13, 2000, 114 Stat. 2338.)

Editorial Notes

Editorial Notes

References in Text
The Federal Food, Drug, and Cosmetic Act, referred to in subsec. (e)(2)(A)(i), is act June 25, 1938, ch. 675, 52 Stat. 1040, which is classified generally to chapter 9 (§301 et seq.) of Title 21, Food and Drugs. For complete classification of this Act to the Code, see section 301 of Title 21 and Tables.