OPINION
HENDLEY, Judge.
Plaintiff, Tommie Hines, received transfusions of blood that came from defendant, Blood Services, Inc., during the course of a special fusion in July, 1970 at St. Joseph’s Hospital. In September, 1970 Hines began treatment for what her doctor diagnosed as “most likely” serum hepatitis. Serum hepatitis can be transmitted by virus infected transfused blood. Hines and her husband sued St. Joseph’s and Blood Services on the theories of strict liability and negligence for the damages cause by the hepatitis. The court granted defendants’ motions for summary judgment on both theories. Plaintiffs appeal.
Strict Liability
Defendants contend that their prima facie showing on strict liability (see Goodman v. Brock, 83 N.M. 789, 498 P.2d 676 (1972)) comes within an exception to the rulé of strict liability. New Mexico has adopted the rule of strict liability stated in Restatement (Second) of Torts, § 402A (1965). Stang v. Hertz Corporation, 83 N.M. 730, 497 P.2d 732 (1972), Garrett v. Nissen Corporation, 84 N.M. 16, 498 P.2d 1359 (1972). The Restatement’s comments recognize an exception to the rule. It states:
“k. Unavoidably unsafe products. There are some products which, in the present state of human knowledge, are quite incapable of being made safe for their intended and ordinary use. These are especially common in the field of drugs. An outstanding example is the vaccine for the Pasteur treatment of rabies, which not uncommonly leads to very serious and damaging consequences when it is injected. Since the disease itself invariably leads to a dreadful death, both the marketing and the use of the vaccine are fully justified, notwithstanding the unavoidable high degree of risk which they involve. Such a product, properly prepared, and accompanied by proper directions and warning, is not defective, nor is it unreasonably dangerous. The same is true of many other drugs, vaccines, and the like, many of which for this very reason cannbt legally be sold except to physicians, or under the prescription of a physician. It is also true in particular of many new or experimental drugs as to which, because of lack of time and opportunity for sufficient medical experience, there can be no assurance of safety, or perhaps even of purity of ingredients, but such experience as there is justifies the marketing and use of the drug notwithstanding a medically recognizable risk. The seller of such products, again with the qualification that they are properly prepared and marketed, and proper warning is given, where the situation calls for it, is not to be held to strict liability for unfortunate consequences attending their use, merely because he has undertaken to supply the public with an apparently useful and desirable product, attended with a known but apparently reasonable risk.”
The uncontradicted evidence in this case establishes that there is a small but medically recognizable risk that transfused blood can transmit serum hepatitis. Also, at the time of Hines’ transfusion, no test could adequately detect the hepatitis virus in blood. Further, no process could destroy it without damaging the blood. At the time of the transfusion in this case, therefore, blood was a product “ * * * which, * * * [was] quite incapable of being made safe for [its] intended and ordinary use. * * * ”
Nonetheless, blood for transfusions is not only “ * * * an apparently useful and desirable product, * * *” it is at times absolutely essential to save life. The risk is outweighed by this public benefit and is thus reasonable.
Plaintiffs do not deny that the blood Hines received was “properly prepared.” They contend that a “proper warning” was not given. They argue that although a written warning of the danger was attached to the blood container, Ms. Hines did not see that warning, nor was she otherwise warned.
The depositions in this case establish that blood is a prescription drug. Ordinarily the manufacturer’s duty to warn of the dangers of prescription drugs is to the attending physician, not the patient. Davis v. Wyeth Laboratories, Inc., 399 F. 2d 121 (9th Cir. 1968); Stottlemire v. Cawood, 213 F.Supp. 897 (D.C.1963); Carmichael v. Reitz, 17 Cal.App.3d 958, 95 Cal.Rptr. 381 (1971). The physician, in turn, has a duty to disclose dangers to the patient. Crouch v. Most, 78 N.M. 406,. 432 P.2d 250 (1967); Woods v. Brumlop, 71 N.M. 221, 377 P.2d 520 (1962). Blood Services placed a warning on the blood container and also “constantly distributed” an “Official Circular of Instructions for Use” to the hospital staff. Dr. Hurley, who gave the transfusion, stated he knew of the danger of hepatitis transmission in blood transfusions. Blood Services’ warning was adequate.
Plaintiffs try to rebut defendants prima facie case by citing Cunningham v. MacNeal Memorial Hospital, 47 Ill.2d 443, 266 N.E.2d 897 (1970) and the reasoning therein. That case held that the exception to the Restatement’s strict liability rule, quoted above, does not apply to the present type of situation since hepatitis infected blood is “impure.” The exception, the court said, “ * * * relates only to products which are not impure and which, even if properly prepared, inherently involve substantial risk of injury to the user. * * * ” On this point Cunningham has been severely criticized. Heirs of Fruge v. Blood Services, 365 F.Supp. 1344 (W.D.La.1973); Brody v. Overlook Hospital, 127 N.J.Super. 331, 317 A.2d 392 (1974); Notes, 69 Mich.L.Rev. 1172 (1971); 24 Vand.L.Rev. 645 (1971); 16 Vill.L.Rev. 983 (1971); 66 N.W.U.L.Rev. 80 (1971); 32 Ohio S.L.J. 585 (1971).
The criticism is well founded. The Cunningham court conveniently ignored a part of the Restatement’s comment which refuted its own contention:
“It is also true in particular of many new or experimental drugs as to which, because of lack of time and opportunity for sufficient medical experience, there can be no assurance of safety, or perhaps even of purity of ingredients, but such experience as there is justifies the marketing and use of the drug notwithstanding a medically recognizable risk. * * *” (Emphasis added)
Although blood cannot be considered a “new or experimental” drug it is new in the sense that no adequate test had been devised to detect the hepatitis virus and even if detected, there is no process to destroy it without damage to the blood. See footnote 1, Brody v. Overlook Hospital, supra.
More importantly the Cunningham court, by categorically limiting the applicability of the exception to “pure” products stultified the flexible policy behind the exception. Instead of a balancing of the dangers of a particular product against its benefits, Cunningham would categorize a large segment of products as vulnerable to strict liability without regard to social benefits.
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OPINION
HENDLEY, Judge.
Plaintiff, Tommie Hines, received transfusions of blood that came from defendant, Blood Services, Inc., during the course of a special fusion in July, 1970 at St. Joseph’s Hospital. In September, 1970 Hines began treatment for what her doctor diagnosed as “most likely” serum hepatitis. Serum hepatitis can be transmitted by virus infected transfused blood. Hines and her husband sued St. Joseph’s and Blood Services on the theories of strict liability and negligence for the damages cause by the hepatitis. The court granted defendants’ motions for summary judgment on both theories. Plaintiffs appeal.
Strict Liability
Defendants contend that their prima facie showing on strict liability (see Goodman v. Brock, 83 N.M. 789, 498 P.2d 676 (1972)) comes within an exception to the rulé of strict liability. New Mexico has adopted the rule of strict liability stated in Restatement (Second) of Torts, § 402A (1965). Stang v. Hertz Corporation, 83 N.M. 730, 497 P.2d 732 (1972), Garrett v. Nissen Corporation, 84 N.M. 16, 498 P.2d 1359 (1972). The Restatement’s comments recognize an exception to the rule. It states:
“k. Unavoidably unsafe products. There are some products which, in the present state of human knowledge, are quite incapable of being made safe for their intended and ordinary use. These are especially common in the field of drugs. An outstanding example is the vaccine for the Pasteur treatment of rabies, which not uncommonly leads to very serious and damaging consequences when it is injected. Since the disease itself invariably leads to a dreadful death, both the marketing and the use of the vaccine are fully justified, notwithstanding the unavoidable high degree of risk which they involve. Such a product, properly prepared, and accompanied by proper directions and warning, is not defective, nor is it unreasonably dangerous. The same is true of many other drugs, vaccines, and the like, many of which for this very reason cannbt legally be sold except to physicians, or under the prescription of a physician. It is also true in particular of many new or experimental drugs as to which, because of lack of time and opportunity for sufficient medical experience, there can be no assurance of safety, or perhaps even of purity of ingredients, but such experience as there is justifies the marketing and use of the drug notwithstanding a medically recognizable risk. The seller of such products, again with the qualification that they are properly prepared and marketed, and proper warning is given, where the situation calls for it, is not to be held to strict liability for unfortunate consequences attending their use, merely because he has undertaken to supply the public with an apparently useful and desirable product, attended with a known but apparently reasonable risk.”
The uncontradicted evidence in this case establishes that there is a small but medically recognizable risk that transfused blood can transmit serum hepatitis. Also, at the time of Hines’ transfusion, no test could adequately detect the hepatitis virus in blood. Further, no process could destroy it without damaging the blood. At the time of the transfusion in this case, therefore, blood was a product “ * * * which, * * * [was] quite incapable of being made safe for [its] intended and ordinary use. * * * ”
Nonetheless, blood for transfusions is not only “ * * * an apparently useful and desirable product, * * *” it is at times absolutely essential to save life. The risk is outweighed by this public benefit and is thus reasonable.
Plaintiffs do not deny that the blood Hines received was “properly prepared.” They contend that a “proper warning” was not given. They argue that although a written warning of the danger was attached to the blood container, Ms. Hines did not see that warning, nor was she otherwise warned.
The depositions in this case establish that blood is a prescription drug. Ordinarily the manufacturer’s duty to warn of the dangers of prescription drugs is to the attending physician, not the patient. Davis v. Wyeth Laboratories, Inc., 399 F. 2d 121 (9th Cir. 1968); Stottlemire v. Cawood, 213 F.Supp. 897 (D.C.1963); Carmichael v. Reitz, 17 Cal.App.3d 958, 95 Cal.Rptr. 381 (1971). The physician, in turn, has a duty to disclose dangers to the patient. Crouch v. Most, 78 N.M. 406,. 432 P.2d 250 (1967); Woods v. Brumlop, 71 N.M. 221, 377 P.2d 520 (1962). Blood Services placed a warning on the blood container and also “constantly distributed” an “Official Circular of Instructions for Use” to the hospital staff. Dr. Hurley, who gave the transfusion, stated he knew of the danger of hepatitis transmission in blood transfusions. Blood Services’ warning was adequate.
Plaintiffs try to rebut defendants prima facie case by citing Cunningham v. MacNeal Memorial Hospital, 47 Ill.2d 443, 266 N.E.2d 897 (1970) and the reasoning therein. That case held that the exception to the Restatement’s strict liability rule, quoted above, does not apply to the present type of situation since hepatitis infected blood is “impure.” The exception, the court said, “ * * * relates only to products which are not impure and which, even if properly prepared, inherently involve substantial risk of injury to the user. * * * ” On this point Cunningham has been severely criticized. Heirs of Fruge v. Blood Services, 365 F.Supp. 1344 (W.D.La.1973); Brody v. Overlook Hospital, 127 N.J.Super. 331, 317 A.2d 392 (1974); Notes, 69 Mich.L.Rev. 1172 (1971); 24 Vand.L.Rev. 645 (1971); 16 Vill.L.Rev. 983 (1971); 66 N.W.U.L.Rev. 80 (1971); 32 Ohio S.L.J. 585 (1971).
The criticism is well founded. The Cunningham court conveniently ignored a part of the Restatement’s comment which refuted its own contention:
“It is also true in particular of many new or experimental drugs as to which, because of lack of time and opportunity for sufficient medical experience, there can be no assurance of safety, or perhaps even of purity of ingredients, but such experience as there is justifies the marketing and use of the drug notwithstanding a medically recognizable risk. * * *” (Emphasis added)
Although blood cannot be considered a “new or experimental” drug it is new in the sense that no adequate test had been devised to detect the hepatitis virus and even if detected, there is no process to destroy it without damage to the blood. See footnote 1, Brody v. Overlook Hospital, supra.
More importantly the Cunningham court, by categorically limiting the applicability of the exception to “pure” products stultified the flexible policy behind the exception. Instead of a balancing of the dangers of a particular product against its benefits, Cunningham would categorize a large segment of products as vulnerable to strict liability without regard to social benefits.
The granting of summary judgment as to Blood Services on strict liability was correct. It follows that under no theory would St. Joseph’s be independently liable under strict liability. The granting of summary judgment as to it was also correct.
Negligence
Plaintiffs in this appeal do not argue that defendant, St. Joseph’s, was in any way negligent or in any way failed to make a prima facie showing for summary judgment. Argument as to this defendant being abandoned, we affirm the judgment in favor of St. Joseph’s.
Defendant, Blood Services, as its prima facie showing on negligence, produced depositions that established: (1) at the time of Hines’ transfusion, donor interviews were the only effective means of screening out hepatitis infected blood; (2) Blood Services extensively interviewed all donors of blood. That showing shifted the burden to plaintiffs. Plaintiffs met that burden with the deposition of Dr. Warren. Both in direct examination and in cross-examination, Dr. Warren stated that the incidence of hepatitis infection is greater with paid donors than with volunteers. Since it is uncontroverted that one of the donors in this case was paid, a genuine issue of fact on the standard of care, breach and causation were raised. See Pribble v. Aetna Life Insurance Company, 84 N.M. 211, 501 P.2d 255 (1972).
Defendants also claim that charitable immunity applies in this case. I do not reach that argument. Section 12-12-5 N.M.S.A. 1953 (Supp.1969), (subsequently amended to § 12-25-5, N.M.S.A. 1953 (Repl.Vol.1968, Poc.Supp.1973)), authorized suits against “ * * * any person, firm, corporation or other organization for negligence. * * * ” Blood Services fits within that enumeration. A negligence suit may validly be brought against them.
The foregoing view on negligence is a minority view and is controlled by the opinion of Judge Lopez concurred in by Judge Hernandez. Accordingly, the order granting summary judgment is affirmed.
It is so ordered.
LOPEZ and HERNANDEZ, JJ, concurring in part and are the majority opinion on the negligence claim.