Opinion
Plaintiff Ronald Shepard appeals from a judgment of dismissal entered after respondent’s demurrers to the complaint and amendment to complaint were sustained without leave to amend.
In his pleadings appellant alleges that he contracted serum hepatitis by reason of a blood transfusion administered to him while he was a patient in respondent hospital.
Asserting that the blood was contaminated with hepatitis virus, appellant sought recovery on alternative theories of strict liability in tort, breach of express and implied warranties, and negligence. 1
Strict Liability in Tort
In California a cause of action for strict liability in tort can be stated under two tests. The first test, laid down in
Greenman
v.
Yuba Power Products, Inc.
(1963)
“(a) the seller is engaged in the business of selling such a product, and
“(b) it is expected to and does reach the user or consumer without substantial change in the condition in which it is sold,
“(2) The rule stated in Subsection (1) applies although
“(a) the seller has exercised ah possible care in the preparation and sale of his product, and
“(b) the user or consumer has not bought the product from or entered into any contractual relation with the seller.” (Italics added.)
As it appears, the two tests are not coextensive. While the Restatement rule requires a sale of the defective product by a seller who is engaged in the business of selling and covers only the user or consumer, the Green-man rale is much broader and imposes strict liability in tort whenever a defective article placed on the market causes injury to a human being. Nevertheless, there is a common denominator in both rules, namely, the requirement of a defective product which, when placed in the stream of commerce, causes injury.
Before examining whether, in light of the foregoing tests, appellant stated a cause of action under strict liability in tort, we ought to emphasize that, appellant’s contention notwithstanding, the question to be decided here is not simply whether human blood is or can be designated as a product under a general definition (cf. Rest.2d Torts, § 402A, com. e;
Cunningham
V.
MacNeal Memorial Hospital
(1970)
In answering this question we need not speculate or make deductions ■ from rales of general applicability. The California Legislature, by statutory enactment, has expressed its intent and declared a clear legal policy that the transfusion of blood and blood product into the human body shall be construed for all purposes to be the rendition of a service and not a sale. Thus, Health and Safety Code, 2 section 1606, provides that “[t]he procure *610 ment, processing, distribution, or use of whole blood, plasma, blood products, and blood derivatives for the purpose of injecting or transfusing the same, or any of them, into the human body shall be construed to be, and is declared to be, for all purposes whatsoever, the rendition of a service by each and every person, firm, or corporation participating therein, and shall not be construed to be, and is declared not to be, a sale of such whole blood, plasma, blood products, or blood derivatives, for any purpose or purposes whatsoever.” (Italics added.)
To underline the legislative intent that a blood transfusion must be considered to be a service even if a sale takes place, section 1600 makes it explicit that the statutory word “distribution” includes sale and exchange (§ 1600.4).
As appellant aptly notes, the rationale behind section 1606 is expressed in
Perlmutter
v.
Beth David Hospital
(1954)
In sum, since section 1606 and its underlying rationale compel the conclusion that a blood transfusion must be regarded as a service, the doctrine of strict liability in tort is inapplicable as a matter of law.
Appellant, however, asks us to extend the doctrine to services. He bases his argument on the broad policy principles enunciated in some cases and voiced by some authorities, and on the salient fact that in a series of cases the doctrine has been extended to a number of nonsale transactions as well.
In justifying the imposition of strict liability the courts have frequently stressed that their purpose is to insure that the cost of injuries resulting from
defective products
are borne by the manufacturers who
put such products on the market
rather than by the injured persons who are powerless to protect themselves
(Greenman
v.
Yuba Power Products, Inc., supra,
at p. 63;
Price
v.
Shell Oil Co.
(1970)
As-indicated before, profound justification exists for the Legislature to determine that a blood transfusion, provided in the course of treatment, should be considered a service rather than a product or sale. It needs no extended discussion to perceive that a hospital is primarily devoted to the care and healing of the sick. The supplying of blood by the hospital is entirely subordinate to its paramount function of furnishing trained personnel and specialized facilities in an endeavor to restore the patient’s health. Providing medicine or supplying blood is simply a chemical aid or instrument utilized to accomplish the objective of cure or treatment. The patient who enters a hospital goes there not to buy medicines or pills, not to purchase bandages, iodine, serum or blood, but to obtain a course of treatment
(Perlmutter
v.
Beth David Hospital, supra,
at pp. 795-796;
Silverhart
v.
Mount Zion Hospital
(1971)
Additional policy considerations also militate against the imposition of strict liability in the situation here presented. Thus, it is widely recognized that despite every effort to screen donors, the possibility that hepatitis virus may be present in the dried plasma cannot be completely obviated. Moreover, if the virus is present, it cannot be discovered by microscopic examination or by any other test known to medical science
(McDaniel
v.
Baptist Memorial Hospital
(6th Cir. 1972)
Appellant’s additional argument that a sale is not, and should not be, a prerequisite to the applicability of strict liability in tort is a far cry from the proposition that it should be extended to services, too.
It is, of course, conceded that subsequent California cases have expanded the scope of the
Greenman
doctrine by imposing strict liability on retail dealers
(Vandermark
v.
Ford Motor Co., supra);
wholesale and retail distributors (Ba
rth
v.
B. F. Goodrich Tire Co.
(1968)
However, it bears special emphasis that a significant element running through all these cases is that “each of the defendants against whom the standard of strict liability has been applied played an integral and vital part in the overall production or marketing enterprise.” (Silverhart v. Mount Zion Hospital, supra, p. 1026; italics added.) This, of course, cannot be said about respondent which was in neither the production nor marketing business of blood. Moreover, it must also be added that there is a strong public policy in favor of promoting an adequate supply of blood. Notwithstanding the danger from latent hepatitis virus, blood transfusions result in a significant net gain in lives (A New Principle of Products Liability in Service Transactions, 30 U.Pitt.L.Rev. 508, supra).
*613
We observe in passing that the cases cited by appellant are all distinguishable from the case at bench and do not call for a different result. Thus, both
Cunningham
v.
MacNeal Memorial Hospital, supra,
and
Jackson
v.
Muhlenberg Hospital
(1969)
Finally, it is worthy of note that shortly after the Illinois Supreme Court held in Cunningham v. MacNeal Memorial Hospital, supra, that a blood transfusion was a sale subjecting the hospital to liability without fault, the Illinois State Legislature adopted a statute exempting hospitals from liability without proving negligence or willful misconduct. In its declaration of policy, the Illinois Legislature said: “The availabilty of scentific knowledge, skills and materials for the purpose of injecting, transfusing or transplanting human whole blood, plasma, blood products, blood derivatives and products, corneas, bones, or organs or other human tissue[ 4 ] is important to the health and welfare of the people of this State. The imposition of liability without fault upon the persons and organizations engaged in such scientific procedures inhibits the exercise of sound medical judgment and restricts the availability of important scientific knowledge, skills and materials. It is therefore the public policy of this State to promote the health and welfare of the people by limiting the legal liability arising out of such scientific procedures to instances of negligence or willful misconduct.” (I ll. Stats., tit. 91, § 181; italics added. See to the same effect: Revised Stat. of Neb., § 71-4809.)
Upon the foregoing reasons we are constrained to adhere to the
*614
time-honored, well-established law which states that those who sell their services for the guidance of others in their economic, financial and personal affairs are burdened only with a duty of reasonable performance under the circumstances and cannot be made liable in the absence of negligence or intentional misconduct
(Gagne
v.
Bertran
(1954)
Warranties
Appellant does not dispute that under existing law sale is an essential element to impose liability under warranties (Cal. U. Com. Code, §§ 2313-2316;
Grinnell
v.
Charles Pfizer & Co.
(1969)
Needless to say, the quoted portion of this latter case brings us back to the same policy considerations which we discussed earlier in deciding whether or not strict liability in tort should attach. It also ought to be emphasized that in cases involving personal injuries resulting from defective products, the theory of strict liability in tort has virtually superseded the concept of implied warranties
(Grinnell
v.
Charles Pfizer & Co., supra,
at p. 432; 13 A.L.R.3d p. 1049). As the court noted in
Greeno
v.
Clark Equipment Company
(N.D.Ind. 1965)
Since, under the foregoing authorities, the liability imposed by strict liability in tort and breach of express and implied warranties is virtually the same, i.e., a form of liability without fault, the conclusion reached in the earlier discussion is equally applicable here.
In addition, the cause of action for alleged breach of express warranty in the case at bench asserts nothing more than the elements of implied warranties. Thus, all that appellant alleges is that: “At said time and place of said sale, and in order to induce plaintiff to purchase said goods, defendants warranted and represented that said blood was of merchantable quality and fit for the purpose intended. Said representations and warranties were a part of the basis of the bargain and sale made between plaintiff and defendants as aforesaid and, in reliance thereon, plaintiff was induced to, and did, purchase said goods as herein above alleged.”
Accordingly, we hold that since the furnishing of a blood transfusion is, by law, a service and not a sale (§ 1606), respondent cannot be held liable under a breach of warranty theory.
The judgment is affirmed.
Taylor, P. J., and Rouse, J., concurred.
Notes
Respondent answered the negligence count at the same time that it demurred to the other causes of action (seven in number). After the trial court sustained the demurrer, appellant dismissed the remaining negligence count without prejudice.
Unless otherwise indicated, ah references will be made to the California Health and Safety Code.
It has been suggested by appellant that greater care in the selection of donors could reduce the likelihood of the presence of hepatitis virus in the blood obtained for use in hospitals, and also that recently ways have been found where the presence of hepatitis can be discovered by application of certain tests (see (1972)
In accord with the policy expressed in this declaration and in harmony with the provisions of section 1606, the California Legislature added section 7155.6 to the code providing that “[t]he use of any human tissue donated pursuant to this chapter [“Uniform Anatomical Gift Act”] for the purpose of transplantation in the human body shall be construed for all purposes as a rendition of a service by each person participating therein and shall not be construed as a sale of such tissue.” (Added by Stats. 1970, ch. 1006, § 3.)
Comment 2 on California Uniform Commercial Code, section 2313, sets forth in part that although this section is limited in its scope and direct purpose to warranties made by the seller to the buyer as part of a contract for sale, the warranty sections of this article are not designed in any way to disturb those lines of case law growth which have recognized that warranties need not be confined either to sales' contracts or to direct parties to such a contract.
