§238q — Title 42 The Public Health and Welfare | U.S. Code

Summary

People who use or try to use an automated external defibrillator (AED) on someone they reasonably believe is having a life‑threatening heart or breathing problem are protected from being sued for harm that happens because of that use. The person or the one who got the AED is also protected unless the harm was caused by the acquirer’s failure to (1) tell local emergency responders where the device was placed within a reasonable time, (2) keep and test the device properly, or (3) give training to the employee who used it — unless that employee would not reasonably be expected to use the device or there was not enough time to train them. The protection does not apply if the harm was caused by intentional criminal acts, very careless or reckless conduct, or a conscious disregard for safety. It also does not cover licensed health professionals using the AED while working in their licensed job, hospitals or health clinics when an employee used the device while working, or an acquirer who leased the device to a health care entity and the entity’s worker caused the harm while working. Perceived medical emergency means a situation where a reasonable person would think an immediate heart or breathing response is needed. AED here means a commercially sold device that detects when a shock is needed and can deliver it automatically. Harm includes physical, emotional, and financial losses. The law does not create a new right to sue, does not force AEDs to be placed, leaves some state rules in place if they already give immunity, keeps existing federal employee protections, and lets state courts handle state‑law cases.

Title 42, §238q

The Public Health and Welfare — Source: USLM XML via OLRC

(a)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 when the employee or agent was the person who used the device on the victim, except that such requirement of training does not apply if—

(A)the employee or agent was not an employee or agent who would have been reasonably expected to use the device; or

(B)the period of time elapsing between the engagement of the person as an employee or agent and the occurrence of the harm (or between the acquisition of the device and the occurrence of the harm, in any case in which the device was acquired after such engagement of the person) was not a reasonably sufficient period in which to provide the training.

(b)Immunity under subsection (a) does not apply to a person if—

(1)the harm involved was caused by willful or criminal misconduct, gross negligence, reckless misconduct, or a conscious, flagrant indifference to the rights or safety of the victim who was harmed;

(2)the person is a licensed or certified health professional who used the automated external defibrillator device while acting within the scope of the license or certification of the professional and within the scope of the employment or agency of the professional;

(3)the person is a hospital, clinic, or other entity whose purpose is providing health care directly to patients, and the harm was caused by an employee or agent of the entity who used the device while acting within the scope of the employment or agency of the employee or agent; or

(4)the person is an acquirer of the device who leased the device to a health care entity (or who otherwise provided the device to such entity for compensation without selling the device to the entity), and the harm was caused by an employee or agent of the entity who used the device while acting within the scope of the employment or agency of the employee or agent.

(c)(1)The following applies with respect to this section:

(A)This section does not establish any cause of action, or require that an automated external defibrillator device be placed at any building or other location.

(B)With respect to a class of persons for which this section provides immunity from civil liability, this section supersedes the law of a State only to the extent that the State has no statute or regulations that provide persons in such class with immunity for civil liability arising from the use by such persons of automated external defibrillator devices in emergency situations (within the meaning of the State law or regulation involved).

(C)This section does not waive any protection from liability for Federal officers or employees under—

(i)section 233 of this title; or

(ii)section 1346(b), 2672, and 2679 of title 28 or under alternative benefits provided by the United States where the availability of such benefits precludes a remedy under section 1346(b) of title 28.

(2)(A)The applicability of subsections (a) and (b) includes applicability to any action for civil liability described in subsection (a) that arises under Federal law.

(B)If a geographic area is under Federal jurisdiction and is located within a State but out of the jurisdiction of the State, and if, pursuant to Federal law, the law of the State applies in such area regarding matters for which there is no applicable Federal law, then an action for civil liability described in subsection (a) that in such area arises under the law of the State is subject to subsections (a) through (c) in lieu of any related State law that would apply in such area in the absence of this subparagraph.

(d)In any civil action arising under State law, the courts of the State involved have jurisdiction to apply the provisions of this section exclusive of the jurisdiction of the courts of the United States.

(e)(1)For purposes of this section, the term “perceived medical emergency” means circumstances in which the behavior of an individual leads a reasonable person to believe that the individual is experiencing a life-threatening medical condition that requires an immediate medical response regarding the heart or other cardiopulmonary functioning of the individual.

(2)For purposes of this section:

(A)The term “automated external defibrillator device” means a defibrillator device that—

(i)is commercially distributed in accordance with the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.];

(ii)is capable of recognizing the presence or absence of ventricular fibrillation, and is capable of determining without intervention by the user of the device whether defibrillation should be performed;

(iii)upon determining that defibrillation should be performed, is able to deliver an electrical shock to an individual; and

(iv)in the case of a defibrillator device that may be operated in either an automated or a manual mode, is set to operate in the automated mode.

(B)(i)The term “harm” includes physical, nonphysical, economic, and noneconomic losses.

(ii)The term “economic loss” means any pecuniary loss resulting from harm (including the loss of earnings or other benefits related to employment, medical expense loss, replacement services loss, loss due to death, burial costs, and loss of business or employment opportunities) to the extent recovery for such loss is allowed under applicable State law.

(iii)The term “noneconomic losses” means losses for physical and emotional pain, suffering, inconvenience, physical impairment, mental anguish, disfigurement, loss of enjoyment of life, loss of society and companionship, loss of consortium (other than loss of domestic service), hedonic damages, injury to reputation and all other nonpecuniary losses of any kind or nature.

Notes & Related Subsidiaries

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.

§238q Liability Regarding Emergency Use of Automated External Defibrillators

Summary

Title 42, §238q

Notes & Related Subsidiaries

Editorial Notes

References in Text

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