Mallinckrodt, Inc. v. Medipart, Inc., and Jerry A. Alexander

976 F.2d 700, 24 U.S.P.Q. 2d (BNA) 1173, 93 Daily Journal DAR 1465, 1992 U.S. App. LEXIS 23367
CourtCourt of Appeals for the Federal Circuit
DecidedSeptember 24, 1992
Docket90-1138, 90-1272
StatusPublished
Cited by114 cases

This text of 976 F.2d 700 (Mallinckrodt, Inc. v. Medipart, Inc., and Jerry A. Alexander) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Mallinckrodt, Inc. v. Medipart, Inc., and Jerry A. Alexander, 976 F.2d 700, 24 U.S.P.Q. 2d (BNA) 1173, 93 Daily Journal DAR 1465, 1992 U.S. App. LEXIS 23367 (Fed. Cir. 1992).

Opinion

PAULINE NEWMAN, Circuit Judge.

This action for patent infringement and inducement to infringe relates to the use of a patented medical device in violation of a “single use only” notice that accompanied the sale of the device. Mallinckrodt sold its patented device to hospitals, which after initial use of the devices sent them to Medi-part for servicing that enabled the hospitals to use the device again. Mallinckrodt claimed that Medipart thus induced infringement by the hospitals and itself infringed the patent.

The district court held that violation of the “single use only” notice can not be remedied by suit for patent infringement, and granted summary judgment of nonin-fringement. 1

The district court did not decide whether the form of the “single use only” notice was legally sufficient to constitute a license or condition of sale from Mallinck-rodt to the hospitals. Nor did the district court decide whether any deficiencies in the “single use only” notice were cured by Mallinckrodt’s attempted subsequent notice, the release of which was enjoined by the district court on the ground that it would harm Medipart’s business. Thus there was no ruling on whether, if the initial notice was legally defective as a restrictive notice, such defect was cured in the subsequent notice. The district court also specifically stated that it was not deciding whether Mallinckrodt could enforce this notice under contract law. These aspects are not presented on this appeal, and the factual premises were not explored at the summary judgment proceeding from which this appeal is taken.

Instead, the district court held that no restriction whatsoever could be imposed under the patent law, whether or not the restriction was enforceable under some other law, and whether or not this was a first sale to a purchaser with notice. This ruling is incorrect, for if Mallinckrodt’s restriction was a valid condition of the sale, then in accordance with General Talking Pictures Corp. v. Western Electric Co., 304 U.S. 175, 58 S.Ct. 849, 82 L.Ed. 1273, 37 USPQ 375, aff'd on reh’g, 305 U.S. 124, 59 S.Ct. 116, 83 L.Ed. 81, 39 USPQ 329 (1938), it was not excluded from enforcement under the patent law.

On review of these issues in the posture in which the case reaches us:

1. The movant Medipart did not dispute actual notice of the restriction. Thus we do not decide whether the form of the restriction met the legal requirements of notice or sufficed as a “label license”, as Mallinckrodt calls it, for those questions were not presented on this motion for summary judgment.

2. Nor do we decide whether Mallinck-rodt’s enjoined subsequent notice cured any flaws in the first notice, for that issue was not reached by the district court.

We conclude, however, on Mallinckrodt’s appeal of the grant of this injunction, that the notice was improperly enjoined.

3. We also conclude that the district court misapplied precedent in holding that there can be no restriction on use imposed as a matter of law, even on the first purchaser. The restriction here at issue does not per se violate the doctrine of patent misuse or the antitrust law. Use in violation of a valid restriction may be remedied under the patent law, provided that no other law prevents enforcement of the patent.

4. The district court’s misapplication of precedent also led to an incorrect application of the law of repair/reconstruction, for if reuse is established to have been validly restricted, then even repair may constitute patent infringement.

BACKGROUND

The patented device is an apparatus for delivery of radioactive or therapeutic material in aerosol mist form to the lungs of a patient, for diagnosis and treatment of pulmonary disease. Radioactive material is delivered primarily for image scanning in diagnosis of lung conditions. Therapeutic *702 agents may be administered to patients suffering various lung diseases.

The device is manufactured by Mallinck-rodt, who sells it to hospitals as a unitary kit that consists of a “nebulizer” which generates a mist of the radioactive material or the prescribed drug, a “manifold” that directs the flow of oxygen or air and the active material, a filter, tubing, a mouthpiece, and a nose clip. In use, the radioactive material or drug is placed in the nebu-lizer, is atomized, and the patient inhales and exhales through the closed system. The device traps and retains any radioactive or other toxic material in the exhálate. The device fits into a lead-shielded container that is provided by Mallinckrodt to minimize exposure to radiation and for safe disposal after use.

The device is marked with the appropriate patent numbers, 2 and bears the trademarks “Mallinckrodt” and “UltraVent” and the inscription “Single Use Only”. The package insert provided with each unit states “For Single Patient Use Only” and instructs that the entire contaminated apparatus be disposed of in accordance with procedures for the disposal of biohazardous waste. The hospital is instructed to seal the used apparatus in the radiation-shielded container prior to proper disposal. The hospitals whose activities led to this action do not dispose of the UltraVent apparatus, or limit it to a single use.

Instead, the hospitals ship the used manifold/nebulizer assemblies to Medipart, Inc. Medipart in turn packages the assemblies and sends them to Radiation Sterilizers Inc., who exposes the packages to at least 2.5 megarads of gamma radiation, and returns them to Medipart. Medipart personnel then check each assembly for damage and leaks, and place the assembly in a plastic bag together with a new filter, tubing, mouthpiece, and nose clip. The “reconditioned” units, as Medipart calls them, are shipped back to the hospitals from whence they came. Neither Radiation Sterilizers nor Medipart tests the reconditioned units for any residual biological activity or for radioactivity. The assemblies still bear the inscription “Single Use Only” and the trademarks “Mallinckrodt” and “UltraVent”.

Mallinckrodt filed suit against Medipart, asserting patent infringement and inducement to infringe. Mallinckrodt also asserted other counts including trademark infringement, unfair competition under section 43(a) of the Lanham Trademark Act, and violation of Illinois unfair competition statutes. Both parties moved for summary judgment on all counts.

The district court granted Medipart’s motion on the patent infringement counts, holding that the “Single Use Only” restriction could not be enforced by suit for patent infringement. The court also held that Medipart’s activities were permissible repair, not impermissible reconstruction, of the patented apparatus. The court reserved for trial Mallinckrodt’s counts of trademark infringement and unfair competition, and entered final judgment on the patent aspects in accordance with Fed. R.Civ.P. 54(b).

The district court also enjoined Mallinck-rodt pendente lite

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976 F.2d 700, 24 U.S.P.Q. 2d (BNA) 1173, 93 Daily Journal DAR 1465, 1992 U.S. App. LEXIS 23367, Counsel Stack Legal Research, https://law.counselstack.com/opinion/mallinckrodt-inc-v-medipart-inc-and-jerry-a-alexander-cafc-1992.