Hegna v. EI DU PONT DE NEMOURS AND CO.

825 F. Supp. 880, 1993 U.S. Dist. LEXIS 9426, 1993 WL 249119
CourtDistrict Court, D. Minnesota
DecidedJuly 8, 1993
DocketCiv. 4-91-678
StatusPublished
Cited by7 cases

This text of 825 F. Supp. 880 (Hegna v. EI DU PONT DE NEMOURS AND CO.) is published on Counsel Stack Legal Research, covering District Court, D. Minnesota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hegna v. EI DU PONT DE NEMOURS AND CO., 825 F. Supp. 880, 1993 U.S. Dist. LEXIS 9426, 1993 WL 249119 (mnd 1993).

Opinion

ORDER

DOTY, District Judge.

This matter is before the court on defendant E.I. du Pont de Nemours and Company’s (“DuPont”) motion for summary judgment on plaintiff Marilyn Hegna’s (“Hegna”) negligence and strict liability claims. In the alternative, DuPont requests that the court reconsider its prior ruling on Hegna’s negligence and strict liability claims in light of .the more fully developed factual record now before the court. Based on a review of the file, record and proceedings herein, the court grants DuPont’s request for reconsideration and determines that summary judgment in favor of DuPont on Hegna’s negligence and-strict liability claims is appropriate;

*882 BACKGROUND

The court set forth many of the facts underlying this action in an order dated November 12,1992. See Hegna v. E.I. du Pont de Nemours and Co., 806' F.Supp. 822 (D.Minn.1992). The court refers to its prior order herein and only summarizes those facts and the procedural history needed to resolve the matters before it.

The present action arises from alleged defects in implants (“TMJ implants”) that Heg-na received during surgery on her temporo-mandibular joints (“TMJ”). Vitek, Inc. 1 (“Vi-tek”) made the implants out of Proplast, a porous and fibrous compound made in an eight-step process in which polytetrafluoroe-thylene (“PTFE”) is mixed with other materials. 2 Vitek purchased its PTFE from DuPont.

Hegna alleges that her implants disintegrated, that PTFE particles from the disintegrated implants caused her injury and that Dupont is liable for those injuries. Hegna claims that DuPont knew of studies questioning the propriety of using PTFE in medical implants and that Vitek was using PTFE to make the TMJ implants. Hegna thus claims that DuPont had a duty to warn her or her physician of the risks involved in using PTFE-based implants, that DuPont failed to provide any warning and that if DuPont had provided a warning, she could have avoided her injuries. Hegna filed this action against DuPont, asserting negligent and strict liability failure to warn claims. 3

DuPont previously moved for summary judgment on Hegna’s negligence and strict liability claims. DuPont argued that Hegna’s negligence claim fails because it merely supplied Vitek with raw materials and played no role in the design, manufacture or sale of the TMJ implants. DuPont argued that it was a bulk supplier and, as such, had no legal duty either to ascertain whether Vitek’s specialized use of PTFE was safe or to warn Hegna or her physician of any potential dangers associated with the use of PTFE in implants. 4 In‘the alternative, DuPont argued that even if it had a duty to warn as a bulk supplier, it satisfied that duty by warning Vitek that PTFE was not made for medical purposes, that it had conducted no tests to determine the efficacy of using PTFE for medical purposes and that Vitek would have to rely on its own medical and legal judgment if it chose to use PTFE to make implants. With respect to the strict liability claim, DuPont argued that Hegna’s claim fails because Vitek’s Proplast manufacturing process altered the chemistry, composition and mechanical properties of the raw PTFE.

The court denied DuPont’s motion for summary judgment on Hegna’s negligence claim. The court, relying in part on Forest v. E.I. DuPont de Nemours & Co., 791 F.Supp. 1460 (D.Nev.1992) and Hill v. Wilmington Chem. Corp., 279 Minn. 336, 156 N.W.2d 898 (1968), determined that DuPont, as a bulk supplier, had a duty to warn at least Vitek of the possible dangers of using PTFE to make TMJ implants and that material' fact disputes concerning the sufficiency of DuPont’s warning precluded summary judgment. See Heg-na, 806 F.Supp. at 826-29. In particular, the court found that

there are material fact disputes concerning whether DuPont knew that Vitek was using PTFE for medical implants, whether Vitek was aware of any potential danger in *883 using PTFE to make implants, whether Vitek materially altered PTFE for such use, whether any disclaimer or warning given to Vitek by DuPont was sufficient to discharge DuPont’s duty and whether DuPont could reasonably rely on Vitek to pass on any such warning.

Id. at 827 (footnotes omitted).

The court also denied DuPont’s motion for summary judgment on Hegna’s strict liability claim. 5 In making that determination, the court noted that:

[t]he distinction between strict liability and negligence in ... failure to warn cases is that in strict liability, knowledge of the condition of the product and the risks involved in that condition will be imputed to the manufacturer, whereas in negligence these elements must be proven.

Id. at 831 (quoting Bilotta v. Kelley Co., 346 N.W.2d 616, 622 (Minn.1984)). The court concluded that:

[i]f Hegna is unable to support her negligence claim at trial by presenting sufficient evidence of DuPont’s knowledge, the court will then determine whether such knowledge should be imputed to DuPont.

Id. at 832.

DuPont now asks the court to reconsider its prior ruling and grant its motion for summary judgment. DuPont renews its argument that as á bulk supplier to Vitek it had no duty to warn Hegna or her physician and had no duty to assure the safety of Vitek’s specialized use of PTFE. DuPont contends that a more developed factual record demonstrates that now there are no material facts in dispute that would preclude summary judgment on Hegna’s negligence and strict liability failure to warn claims." In the alternative, DuPont raises two new arguments in support of its summary judgment motion. First, DuPont contends that Heg-na’s claims are preempted by 21 U.S.C. § 360k of the Medical Device Amendments. Second, DuPont contends that the applicable statute of limitations bars Hegna’s strict liability claim.

DISCUSSION

Rule 56(c) of the Federal Rules of Civil Procedure provides that summary judgment “shall be rendered forthwith if the pleadings, depositions, answers to interrogatories, and admissions on file, together with affidavits, if any, show that there is no genuine issue as to any material fact and that the moving party is entitled to a judgment as a matter of law.” This standard mirrors the standard for a directed verdict under Federal Rule of Civil Procedure

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Bluebook (online)
825 F. Supp. 880, 1993 U.S. Dist. LEXIS 9426, 1993 WL 249119, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hegna-v-ei-du-pont-de-nemours-and-co-mnd-1993.