■ MEMORANDUM
This case has been assigned to me for final disposition, with the consent of the parties.
1
Local Rule 301.4; 28 U.S.C. § 636(c). Currently ripe for resolution is the motion for summary judgment filed by defendant Baxter Healthcare Corporation (“Baxter”), which has been fully, indeed too-fully, briefed.
2
(Papers No. 22, 23, 26, 28, 33, 36, and 37.) No hearing is necessary. Local Rule 105.6;
Sakaria v. TWA,
BACKGROUND
This lawsuit stems from surgery the plaintiff, Ms. Kelly Miskin (“Miskin”), underwent in April 1983, during which silicone filled implants were inserted into her breasts. She originally filed suit in this court in October 1992, but in March 1993, the case was transferred to the Northern District of Alabama as part of multidistrict litigation proceedings. By order dated March 2, 1998, the case was remanded to this court for all further proceedings. (Paper No. 8.) Plaintiffs second amended complaint, (Paper No. 3), asserts the following causes of action against Baxter, and Mentor Corporation, its co-defendant 3 : negligence, strict liability, fraud, failure to warn, intentional infliction of emotional distress, negligent infliction of emotional damages, and breach of implied warranty. (Second Am. Compl., Paper No. 3.) All of these causes of action turn on the plaintiffs claim that her implants were defective and caused her to develop Crohn’s syndrome, and suffer other physical and emotional injuries. Because the surgery during which the breast inserts were in *671 stalled took place in Maryland, the parties agree that Maryland law controls the substantive issues in this case. (Paper No. 42) (order directing counsel to inform the court if they contend that law other than Maryland law controls substantive issues).
The essence of Baxter’s motion is that plaintiff has failed to meet her burden during summary judgment practice to identify evidentiary facts sufficient to create a genuine issue of material fact with respect to product defect, and causation. According to Baxter, the plaintiff has failed to identify admissible evidence which will be provided by any expert to establish that the implants in question were' defective, or that they caused the injuries plaintiff claims. Because I agree, I will enter summary judgment in behalf of Baxter.
LEGAL ANALYSIS
The law is well settled that summary judgment is mandated if the non-moving party fails to make a showing sufficient to establish the existence of an element essential to that party’s case, on which he or she bears the burden of proof. Fed. R.Civ.P. 56(c);
Celotex Corp. v. Catrett,
Moreover, a mere scintilla of supporting evidence is not enough to defeat a summary judgment motion. The non-moving party must identify sufficient evidence that reasonable jurors could find by a preponderance of the evidence.
See Anderson,
With respect to the substantive law which controls the outcome of the pending motion, it is clear that Maryland law requires the plaintiff to produce evidence that the implants were defective, and that this was the proximate cause of the injuries she claims.
Lee v. Baxter Healthcare Corp.,
DISCUSSION
In response to Baxter’s challenge, plaintiff has identified the following sources of evidence to support her defect and causation claims: (1) Irving Brick, MD, a treat *673 ing physician; (2) Sanford Richmond, MD, a treating physician; (3) two untitled, unauthenticated, medical treatises; (4) a list of sixteen unauthenticated documents, containing no description of the contents of the documents; (5) Dr. Klein, a treating psychiatrist, who was first identified, but than later withdrawn, as a source of testimony at trial; (6) Casaba Magassy, MD, the surgeon who originally did the insert surgery on plaintiff; (7) seven “experts,” for whom no Fed.R.Civ.P. 26(a)(2)(B) disclosures, affidavits, or transcripts of deposition or trial testimony were furnished, (8) a list of 18 non-treating, “experts” who have testified in connection with other breast implant cases, and (9) a list of nine “experts,” first identified in a paper filed as part of the briefing of this motion on June 16, 1999, 4 long after the close of discovery, 5 and without any Rule 26(a)(2)(B) disclosures, summary of expected testimony, affidavits, or excerpts from deposition or trial testimony. As next will be seen, taken individually, and collectively, the facts which the plaintiff has identified to create triable issues regarding product defect and causation do not amount to evidentiary facts, and fall far short of what is needed to meet Baxter’s summary judgment challenge.
1. Irving Brick, MD.
Dr. Brick was identified by the plaintiff as a trial witness in a “supplemental” witness designation, and in a letter from plaintiffs counsel to Baxter’s counsel. (Def.’s Reply Mem., Ex. 1 & 2, Paper No. 26.) These designations contain no description of what Dr. Brick would testify to at trial, and no affidavits or deposition or trial testimony excerpts were provided. Thus, as to Dr. Brick, plaintiff has failed to produce any evidentiary facts to challenge Baxter’s motion.
2. Sanford Richman, MD.
As to Dr. Richman, plaintiffs treating physician, she has identified three sources of information regarding his expected trial testimony; a letter dated October 13, 1993 ( Pl.’s Opp’n Mem., Ex. A, Paper No. 23); a letter dated May 4, 1994 (Pl.’s Opp’n Mem., Ex. B, Paper No. 23); and citation to his deposition testimony of May 24, 1999 (Pl.’s Supplemental Mem., Paper No. 36; Def.’s Surreply Mem., Ex. A, Paper No. 33). The October 13, 1993 letter is unsworn and unauthenticated, making it inappropriate for consideration during summary judgment.
See Orsi,
Dr. Richman’s May 4,1994 letter is similarly deficient. It is unsworn and unauthenticated, and merely recites the plaintiffs symptoms and the care he has given her. The letter is silent about defect or causation, and therefore is of no evidentia-ry value on these issues. Finally, the excerpts of Dr. Richman’s deposition testimony which were cited by the parties are substantively insufficient to create a triable issue on defect or causation. For example, at page 12 of his deposition, Dr. *674 Richman testified that he did not have an opinion, to a reasonable degree of medical probability, that a relationship existed between plaintiffs silicone breast implants and her Crohn’s disease, acknowledging that he only thought there was a possible relationship, and that he did not feel strongly about this. Further, he testified that he told plaintiffs counsel that he was not qualified to serve as a retained expert in this case, because he lacked the necessary research credentials. 6 Further, when asked whether it would be fair to say that if he should testify at trial, he would not express the opinion that plaintiffs Crohn’s disease was caused by her silicone breast implants, he answered: “No. I would not offer that opinion”. (Def.’s Surreply Mem., Ex. A at 145-46, Paper No. 33.)
In her final briefing, (Paper No. 36), plaintiff quotes — but fails to attach an excerpt of the deposition transcript — Dr. Richman as testifying in his deposition that “I think that I would be willing to say that most of the evidence points to Crohn’s disease being caused by a autoimmune process. I’m not a hundred percent certain of that. But within the realm of probability in terms of what most physicians believe today, it probably is caused by an autoimmune process”. Even if this conclusory opinion, offered without any of the foundational facts which are required to enable the court to determine, pursuant to Fed.R.Evid. 104(a), 702 and 703, whether it would even be admissible, 7 is accepted as true, it still falls far short of the mark. The opinion offers no nexus between the plaintiffs implants and any autoimmune injury, and further is silent with regard to any defect in the implants themselves. Thus, from a review of all of the sources of Dr. Richman’s opinions which have been made a part of the record in this case, no admissible evidence has been identified which would support the plaintiffs theories of defect and causation.
3. Medical treatises, list of documents.
Plaintiff attached as exhibit C to her opposition memorandum, (Paper No. 23), two unauthenticated medical treatises, one of which was also unidentified. To be considered, they would have to be shown to be admissible in evidence. Thus, there would have to be some evidence to show that they are authentic, as Fed.R.Evid. 901 requires, and, if they are to be considered for their substantive value, that they qualify as learned treatises under Fed.R.Evid. 803(18). These foundational facts are entirely lacking, making the treatises unauthenticated, inadmissible hearsay, which cannot be considered during summary judgment.
Similarly, the list of sixteen documents identified by plaintiff to support her defect and causation claims, (Pl.’s Opp’n Mem., Ex. D, Paper No. 23), is inadmissible. The exhibit simply lists the documents by date, giving only a brief description of each document. There is no affidavit or other authenticating information, the documents themselves were not attached, nor was any *675 summary of their contents. The list is therefore inadmissible, Fed.R.Evid. 901, 802, and may not be considered during summary judgment practice.
k- Doctors Klein and Magassy.
In a letter dated April 15, 1999, plaintiffs counsel informed defendant’s counsel that Dr. Klein would not be offered as a trial witness because he had no views on the medical issues in the case. (Def.’s ■ Reply Mem., Ex. 2, Paper No. 26.) Nothing further was provided regarding any opinions Dr. Klein may have. There is nothing of evidentiary value, therefore, which he contributes to summary judgment analysis.
Similarly, while plaintiff identified Dr. Casaba Magassy, her treating surgeon, as a trial witness in her supplemental witness designation, no proffer of his testimony was included, nor was any affidavit provided by the plaintiff, or any excerpt from deposition testimony. Instead, the defendants produced an affidavit from Dr. Ma-gassy, 8 in which he stated that he has not agreed to act as an expert witness for the plaintiff, and disclaims any opinion to a reasonable degree of medical certainty that plaintiffs implants had any defect which caused her any injury. (Def.’s Reply Mem., Ex. 3, Paper No. 26.) Plaintiff offered nothing in response to this affidavit. Accordingly, Dr. Magassy offers no support for her defect and causation theories.
5. Plaintiff’s “supplemental” designation of experts.
After Baxter filed its summary judgment motion, plaintiff submitted two separate supplemental” expert designations. The first, dated April 3, 1999, identified seven experts who previously had provided deposition and/or trial testimony in other silicone implant cases. (Def.’s Reply Mem., Ex. 1, Paper No. 26.) Despite the fact that all seven had previously testified, plaintiff failed to attach any transcript excerpts to establish what their testimony would be, nor did she even summarize what their prior testimony was. As the cases cited above establish, this is not sufficient during summary judgment to carry the plaintiffs burden to show triable issues of fact with respect to each essential element of her claims. Accordingly, the seven additional experts identified by name only on April 3, 1999, provide no support for plaintiffs position at summary judgment.
Similarly, on May 4, 1999, plaintiff filed a supplemental response to the defendant’s motion. (Paper No. 28.) Attached at exhibit A is a supplemental designation of expert witnesses, listing eighteen experts, none of whom were treating physicians, and outlining the testimony each might provide at trial. While the summaries give some idea what each expert might say at trial, they are nonetheless general, often vague, and not tailored to the specifics of the plaintiffs claims in this case. Further, as non-treating physicians, each of these experts was subject to the disclosure requirements of Rule 26(A)(2)(B). 9 None of the disclosures meets these requirements, either in substance, or in form, further depriving this court of the ability to assess *676 whether the proffered testimony would be admissible at trial. Similarly, the plaintiff failed to provide affidavits or excerpts from deposition/trial testimony with respect to any of the eighteen additional retained experts, thus failing to provide any facts from which this court could determine whether the proffered testimony would be admissible at trial. Accordingly, as discussed above, the designation of the eighteen additional experts fails to support the plaintiffs position at the summary judgment stage.
6. Plaintiff’s final designation of Nine “experts”.
In Paper No. 36, plaintiffs final supplemental summary judgment submission, she identifies by name and case title nine experts who provided testimony in other breast implant cases on the issue of causation. As repeatedly stated above, identification of these experts by name alone, with no proffer of expected testimony, affidavit, or transcript excerpt, adds nothing to sustain plaintiffs burden of establishing triable issues of defect and causation.
In summary, analyzed individually, and collectively, each of the sources of evidence of product defect and causation identified by the plaintiff in her summary judgment papers fails to meet the long established summary judgment standards, discussed above. Plaintiff has, accordingly, failed to meet her burden to show that there are triable issues of fact regarding product defect, and causation. Without proof of these two elements, each of the plaintiffs claims fails, and for this reason, defendant is entitled to summary judgment. 10 A separate order shall issue.
Notes
. On November 18, 1998, the parties initially agreed to a provisional consent to proceed before a United States Magistrate Judge, including consent to proceed before a United States Magistrate Judge for dispositive pretrial matters. (Paper No. 18.) However, in August 1999, all parties agreed to proceed before a United States Magistrate Judge for all proceedings in the case, including trial and entry of a final judgment. Judge William Nickerson signed an order referring this case to the undersigned for all proceedings on August 31, 1999.
. Local Rule 105.2.a prohibits the filing of surreply memoranda without approval of the court. Both parties in this case ignored this rule, and filed surreplies. Ordinarily I would not consider these briefings. However, in this case I will do so in order to fully dispose of the issues raised. Counsel are forewarned that, in future cases, if unauthorized surre-plies are filed, they may well be disregarded by the court.
. Baxter asserts in its motion papers that Mentor Corporation was never served. Plaintiff does not argue otherwise, and there is no record of service in the court file. The implants which are the subject of this case allegedly were manufactured by Heyer-Schulte Corporation, a wholly owned subsidiary of American Hospital Supply Corporation. In March 1984, American Hospital sold its breast implant product line to Mentor Corporation, and in the process American Hospital agreed to indemnify Mentor for any liability arising out of implants manufactured by Hey-er-Schulte. In November 1985, American Hospital was acquired by Baxter Travenol Laboratories, Inc. In December 1988, American Hospital merged into Travenol Laboratories, and this entity is now called Baxter Healthcare Corporation.
Lee v. Baxter Healthcare Corp.,
. Plaintiff's supplemental memorandum (Paper No. 36.)
. The amended scheduling order issued by Judge Nickerson imposed a discovery cutoff of April 30, 1999, and set a trial date of September 13, 1999. (Am. Scheduling Order, Paper No. 15.)
. As a treating physician, it would still be possible to identify Dr. Richman as a trial witness; and to have him express admissible opinions even if he was not offered as a retained expert. Fed.R.Civ.P. 26(a)(2)(A);
see also Sullivan v. dock,
.
See Daubert v. Merrell Dow Pharmaceuticals, Inc.,
. To be considered on summary judgment, an affidavit must affirmatively show that the affi-ant is competent to testify, and has personal knowledge of the facts sworn to. Fed. R.Civ.P. 56(e ). Dr. Magassy's affidavit fails to recite that he has personal knowledge of the facts contained therein. However, because the facts derive from his role as the doctor who performed the surgery in which the plaintiff's breast implants were inserted, its clear that he does have personal knowledge, as required.
. Both by the requirements of the rule itself, as well as an order of the multidistrict court, "Appendix B to order no. 30 (CV 92-P-10000-S) Retained Experts — Disclosure, Discovery and Testimony." ( PL's Supplemental Resp., Ex. A, Paper No. 28.) This order clearly provides at paragraph 2(A) that retained experts' reports must comply with the requirements of Rule 26(A)(2). That rule requires, at subsection (B), that comprehensive disclosures be provided in written reports signed by each retained expert.
. Plaintiff argues in her final submission, (Paper No. 36), that even if her claims for injuries associated with Crohn’s disease do not survive summary judgment, she has nonetheless established that her claims for pain and suffering, and mental anguish must survive. However, this is so only if she has presented sufficient evidentiary facts to establish product defect, and a causal nexus with each of her asserted non-Crohn's disease injuries. As the above analysis demonstrates, she has failed to do so. Thus, none of her claims for injuries can survive summary judgment.
