Douglass v. NTI-TSS, INC.

632 F. Supp. 2d 486, 2009 U.S. Dist. LEXIS 58258, 2009 WL 1955771
CourtDistrict Court, D. Maryland
DecidedJuly 6, 2009
DocketCivil CCB-09-558
StatusPublished
Cited by9 cases

This text of 632 F. Supp. 2d 486 (Douglass v. NTI-TSS, INC.) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Douglass v. NTI-TSS, INC., 632 F. Supp. 2d 486, 2009 U.S. Dist. LEXIS 58258, 2009 WL 1955771 (D. Md. 2009).

Opinion

MEMORANDUM

CATHERINE C. BLAKE, District Judge.

Now pending is a motion to dismiss filed by the defendant, NTI-TSS, Inc. (“NTI”), against the plaintiff, Holly Douglass (“Ms. Douglass”). Ms. Douglass’s claims involve injuries she allegedly sustained using NTI’s product and are based on the defendant’s alleged failure to warn of the known risks associated with the product. NTI moves to dismiss the majority of the plaintiffs claims as time-barred by Maryland’s statute of limitations, and seeks dismissal of the remaining claims for failure to allege sufficient facts to state a claim for which relief can be granted. The issues have been fully briefed and no hearing is necessary. For the following reasons, the defendant’s motion will be granted.

BACKGROUND

The plaintiff, Ms. Douglass, was a patient of William DeLong, D.D.S. (“Dr. DeLong”). On or about April 21, 2003, Dr. DeLong prescribed and fitted Ms. Douglass with a partial coverage mouth guard manufactured by the defendant, NTI, to be worn nightly. The mouth guard was intended to prevent or reduce headaches caused by temporomandibular joint dysfunction, known as TMJ, and to reduce or eliminate tooth damage caused by nighttime teeth grinding. Dr. DeLong did not warn Ms. Douglass of risks or dangers of using the mouth guard, in particular the risk of developing an open anterior bite, nor did he obtain informed consent from Ms. Douglass.

On or about February 25, 2004, Ms. Douglass complained to Dr. DeLong of various symptoms, including that she was talking differently and having difficulty eating because her front teeth did not meet together when she bit down. She later complained to Dr. DeLong of migraine-type headaches. Dr. DeLong diagnosed Ms. Douglass with severe open anterior bite, which “involves shifting of the entire lower jaw, or the movement of teeth in the posterior portion of the mouth, so that the upper and lower teeth in the anterior or front of the mouth no longer contact each other, causing an open bite” (Compl. ¶ 7). As a result of developing the condition, the plaintiff has had to undergo significant and costly diagnostic and treatment services, and has suffered physical and emotional injury.

The plaintiff began investigating the cause of her condition approximately ten months after her diagnosis. On December 31, 2004, she found statistics on NTI’s website indicating that 5% of patients develop open anterior bite along with a statement that dentists prescribing the product should warn patients of this potential risk and obtain patients’ informed consent. Over one year later, in early 2006, Ms. Douglass’s attorney wrote to NTI alleging that its product was defective and unreasonably dangerous due, in part, to the failure to warn plaintiff of the possibility of developing open anterior bite. The letter also stated plaintiffs belief that NTI was legally liable for her injuries. According to the complaint, counsel for NTI replied in a March 3, 2006 letter (“March 2006 letter”), stating that “in early 2003[NTI] had warned Dr. DeLong about the danger of open anterior bite, because it had provided literature and an instructional videotape discussing this possibility, which it supplied with the actual mouth guard that was shipped to the dentist.” (Id. ¶ 21.)

The defendant has attached a copy of the March 2006 letter to its motion to *490 dismiss. 1 The letter states that “[w]hen [NTI] ships product to practitioner dentists informational material accompanying the treatment kits ... explain how the device works and that a rare number of patients develop an anterior open bite following use of the device. The dental practitioner is advised to explain this potentiality to the patient, make sure that the patient understands it and have the patient sign an informed consent form.” (Def.’s Mem. Ex. B at 2.) The letter also expressed “surprise[] that Dr. DeLong did not discuss with Ms. Douglass the potential development of an anterior open bite” and suggested that “Dr. DeLong’s chart should contain an informed consent form signed by Ms. Douglass.” (Id. at 1.) The letter concluded with the following passage: “If this information is news to you or Ms. Douglass and if there are no notes in Dr. DeLong’s chart advising Ms. Douglass of how the [NTI] device works I submit that the cause of Ms. Douglass’ present symptomology does not lie at the feet of [NTI] but perhaps elsewhere.”

Approximately ten months after receiving the letter, in January 2007, the plaintiff submitted a claim to Maryland’s Health Care Alternative Dispute Resolution Office (“HCADRO”) alleging that Dr. DeLong was negligent for failing to obtain her informed consent. In October 2007, the pending case was transferred to the Circuit Court for Howard County at the request of Dr. DeLong. In late 2007 or early 2008, plaintiffs counsel was told by Dr. DeLong’s attorney that Dr. DeLong never received any informational material from NTI regarding open anterior bite and that he was not aware of the risk associated with the defendant’s product.

According to the complaint, in the fall of 2008, the plaintiffs attorney initiated phone conversations with NTI and, during those conversations, received further assurances from NTI’s attorney that the company had provided warnings about open anterior bite to Dr. DeLong. During these phone conversations, the plaintiffs attorney requested that NTI provide a witness to testify to the defendant’s practices in warning dentists about open anterior bite, but “the defendant’s attorney never fully responded to the requests.” (Compl. ¶ 27.)

Thereafter, new counsel for Dr. DeLong spoke with an NTI representative and “was informed or led to believe that the defendant did not issue warnings about the danger of open anterior bite until sometime after the plaintiff developed the condition.” (Id. ¶ 28). Upon receiving this information from Dr. DeLong’s attorney, Ms. Douglass filed the present suit in state court on December 31, 2008, alleging negligence in Count I, willful and wanton misconduct in Count II, strict products liability in Count III, breaches of express and implied warranties in Count TV, fraud in Count V, and negligent misrepresentation in Count VI. The defendant timely removed the action to this court and filed the pending motion to dismiss.

ANALYSIS

“The purpose of a Rule 12(b)(6) motion is to test the sufficiency of a complaint; importantly, a Rule 12(b)(6) motion does *491 not resolve contests surrounding the facts, the merits of a claim, or the applicability of defenses.” Edwards v. City of Goldsboro, 178 F.3d 231, 243 (4th Cir.1999) (internal quotation marks and alterations omitted). When ruling on such a motion, the court must “accept the welkpled allegations of the complaint as true,” and “construe the facts and reasonable inferences derived therefrom in the light most favorable to the plaintiff.” Ibarra v. United States, 120 F.3d 472, 474 (4th Cir.1997). Following the Supreme Court’s ruling in Bell Atlantic Corp. v. Twombly,

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632 F. Supp. 2d 486, 2009 U.S. Dist. LEXIS 58258, 2009 WL 1955771, Counsel Stack Legal Research, https://law.counselstack.com/opinion/douglass-v-nti-tss-inc-mdd-2009.