Depowski v. Suburban Surgical Care Specialists, S.C.

2025 IL App (1st) 231465-U
Appellate Court of Illinois·Decided September 19, 2025·No. 1-23-1465·Unpublished

Opinion

No. 1-23-1465

2025 IL App (1st) 231465-U No. 1-23-1465

Order filed September 19, 2025 FIFTH DIVISION

NOTICE: This order was filed under Supreme Court Rule 23 and is not precedent except in the limited circumstances allowed under Rule 23(e)(1).

IN THE

APPELLATE COURT OF ILLINOIS FIRST JUDICIAL DISTRICT

MARIANNE L. DEPOWSKI, ) Appeal from the ) Circuit Court of

Plaintiff-Appellant, ) Cook County, ) Law Division

v. )

) No. 2018L3414

SUBURBAN SURGICAL CARE SPECIALISTS, )

S.C., and JONATHAN W. WALLACE, M.D., ) Honorable ) Elizabeth M. Budzinski, Defendants-Appellees. ) Judge, presiding.

PRESIDING JUSTICE MITCHELL delivered the judgment of the court.

Justice Mikva and Justice Oden Johnson concurred in the judgment.

ORDER

¶1 Held: The circuit court’s judgment entered on a jury verdict in favor of the defendants is affirmed where the circuit court did not abuse its discretion in excluding irrelevant expert testimony and did not err in striking res ipsa loquitur claims where the doctrine did not apply.

¶2 Following a jury trial and defense verdict in this medical malpractice case, plaintiff Marianne Depowski appeals contending that a series of trial court rulings require a new trial. The case arises from a claim of negligence alleging that defendant Dr. Jonathan Wallace failed to remove a small plastic tube during a procedure to remove a gastric band. Specifically, plaintiff raises the following issues: (1) Did the circuit court err in striking plaintiff’s res ipsa loquitur

No. 1-23-1465

counts because retention of a foreign body in a patient has been characterized as a “never event”? (2) Did the circuit court abuse its discretion in barring expert testimony based on an untimely disclosure where it did not apply the factors for determining whether to exclude testimony as a sanction for violating discovery rules? (3) Did the circuit court abuse its discretion in barring plaintiff’s expert from offering an opinion as to whether defendant doctor knew or should have known about an FDA recall where plaintiff timely disclosed it? Because we conclude that plaintiff’s contentions of error are either unsupported in law or without a basis in the record, we affirm.

¶3 I. BACKGROUND

¶4 In 2008, plaintiff Marianne Depowski went to defendants Suburban Surgical Care and Jonathan Wallace, M.D., for help losing weight. After a consultation, defendant doctor installed a gastric band device around plaintiff’s stomach. There were no issues with the surgery to install the device, and plaintiff was happy with the results.

¶5 In 2010, the Food and Drug Administration required the device’s manufacturer to issue a recall because a portion of tubing could detach from the device and migrate inside the patient’s body. The recall notice issued to consignees of the device so they could avoid installing any additional devices. The recall did not require previously installed devices to be removed, and the FDA did not require all doctors who had installed a recalled device to be notified. Defendant doctor was not a consignee and maintained at trial he had not otherwise been informed of the recall.

¶6 In 2015, the device inside plaintiff began to erode, causing an infection and considerable pain. This type of erosion was a known issue that occurred with a small number of gastric bands and was not related to the recall or the 2008 surgery. Plaintiff returned to defendant doctor to have

No. 1-23-1465

the device removed. He performed the extraction with the assistance of a physician’s assistant and a scrub nurse.

¶7 By the time of the extraction surgery, while most of the device remained intact, the defect had caused the tubing to separate from the rest of the device. Tissue buildup on the device obscured that the tubing had detached. Therefore, although defendant doctor intended to remove the complete device, the tubing remained in plaintiff’s abdomen. Over the next year, plaintiff’s pain continued. In 2017, a surgeon at another hospital determined that the cause of the pain was the tube that had been left behind and performed surgery to remove it.

¶8 Plaintiff filed a complaint against defendants alleging both specific negligence and negligence under a theory of res ipsa loquitur. At trial, defendants did not contest plaintiff’s account of what happened during the 2015 surgery, instead focusing on whether the standard of care was violated and the proximate cause of plaintiff’s injuries. Both plaintiff and defendants offered expert witnesses, Dr. Emma Patterson and Dr. Sidney Rohrscheib, respectively. The circuit court excluded Dr. Patterson’s testimony about how she learned of the FDA recall, struck the res ipsa loquitur counts, and instructed the jury only on negligence. The jury returned a general verdict for defendants. Plaintiff filed a motion for a new trial that the circuit court denied. This timely appeal followed. Ill. S. Ct. R. 303 (eff. July 1, 2017).

¶9 II. ANALYSIS

¶ 10 A. Exclusion of Expert Testimony on “Never Events”

¶ 11 Plaintiff asserts that the circuit court improperly barred expert testimony from plaintiff’s expert, Dr. Emma Patterson, because the circuit court did not apply the relevant factors in deciding whether to bar the testimony as untimely under Illinois Supreme Court Rule 213(f)(3) (eff. Jan. 1, 2018). Sullivan v. Edward Hospital, 209 Ill. 2d 100, 110 (2004) (outlining the factors courts must

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consider “[i]n determining whether the exclusion of a witness is a proper sanction for nondisclosure”). Defendants argue the circuit court never barred any testimony from Dr. Patterson that “never events” did not ordinarily occur in the absence of negligence because plaintiff never offered it. We review the exclusion of a witness due to improper disclosure under Rule 213 for an abuse of discretion. Id. at 109.

¶ 12 Plaintiff claims to have sought to offer expert testimony from Dr. Patterson that what occurred here constituted a “never event” to support the application of the res ipsa loquitur doctrine. Defendants moved in limine to bar testimony as to res ipsa loquitur and “never events.” The doctrine “allow[s] proof of negligence by circumstantial evidence when the direct evidence concerning cause of injury is primarily within the knowledge and control of the defendant.” Metz v. Central Illinois Electric & Gas Co., 32 Ill. 2d 446, 449 (1965). To avail herself of res ipsa loquitur, a plaintiff “must plead and prove that [she] was injured (1) in an occurrence that ordinarily does not happen in the absence of negligence (the probability element) (2) by an agency or instrumentality within the defendant’s exclusive control (the control element).” Johnson v. Armstrong, 2022 IL 127942, ¶ 35.

¶ 13 Here, the probability element turned on testimony by Dr. Patterson as to “never events” that plaintiff argues was improperly barred. A “never event” is a “serious reportable event” as classified by the National Quality Forum, such as operating on the wrong patient. Plaintiff argues Dr. Patterson’s opinion as to “never events” was disclosed in a letter sent to defendants after the discovery deadline informing defendants that Dr. Patterson agreed with general statements from defendants’ expert as to “never events.”

¶ 14 In its order denying plaintiff’s posttrial motion, the circuit court made clear that it “struck the res ipsa loquitur counts because Plaintiff did not disclose that her expert would testify that this

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alleged malpractice, ‘ordinarily would not occur in the absence of negligence’ and Plaintiff’s expert never so testified in her deposition.” The circuit court underscored that “no such evidence was presented.” Even in the untimely disclosures, plaintiff never disclosed an opinion that “never events” did not ordinarily occur in the absence of negligence. At most, plaintiff stated in her letter that Dr. Patterson agreed with defendants’ expert’s statement that no reasonably careful surgeon would “do any of the things listed in the never events.”

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