97-17152. Joseph M. Piacentile, M.D.; Revocation of Registration  

  • [Federal Register Volume 62, Number 126 (Tuesday, July 1, 1997)]
    [Notices]
    [Pages 35527-35529]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-17152]
    
    
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    DEPARTMENT OF JUSTICE
    
    Drug Enforcement Administration
    [Docket No. 96-37]
    
    
    Joseph M. Piacentile, M.D.; Revocation of Registration
    
        On June 25, 1996, the Deputy Assistant Administrator, Office of 
    Diversion Control, Drug Enforcement Administration (DEA), issued an 
    Order to Show Cause to Joseph M. Piacentile, M.D., (Respondent) of 
    Yardley, Pennsylvania and Basking Ridge, New Jersey, notifying him of 
    an opportunity to show cause as to why DEA should not revoke his DEA 
    Certificates of Registration, BP1786853 and BP2526056, pursuant to 21 
    U.S.C. 824 (a)(4) and (a)(5), and deny any pending applications for 
    renewal of such registrations as a practitioner under 21 U.S.C. 823(f).
        By letter dated July 15, 1996, Respondent, proceeding pro se, filed 
    a request for a hearing, and following prehearing procedures, a hearing 
    was held in New York, New York on November 20, 1996, before 
    Administrative Law Judge Gail A. Randall. At the hearing, the 
    Government called a witness to testify and introduced documentary 
    evidence. Respondent made a brief opening statement, but did not 
    testify under oath nor offer any documentary evidence. After the 
    hearing, Government counsel and Respondent submitted proposed findings 
    of fact, conclusions of law and argument. On March 26, 1997, Judge 
    Randall issued her Opinion and Recommended Ruling, recommending that 
    Respondent's DEA Certificates of Registration be revoked. Neither party 
    filed exceptions to her decision, and on May 5, 1997, Judge Randall 
    transmitted the record of these proceedings to the Acting Deputy 
    Administrator.
        The Acting Deputy Administrator has considered the record in its 
    entirety, and pursuant to 21 CFR 1316.67, hereby issues his final order 
    based upon findings of fact and conclusions of law as hereinafter set 
    forth. The Acting Deputy Administrator adopts, in full, the Opinion and 
    Recommended Ruling of the Administrative Law Judge, and his adoption is 
    in no manner diminished by any recitation of facts, issues and 
    conclusions herein, or of any failure to mention a matter of fact or 
    law.
        The Acting Deputy Administrator finds that Respondent is currently 
    registered with DEA in both Pennsylvania and New Jersey. In January 
    1985, the Department of Health and Human Services, Office of the 
    Inspector General initiated an investigation of Electro Therapeutics 
    (ETI) after receiving hundreds of complaints from Medicare patients 
    concerning medical equipment they had received from ETI. Respondent was 
    the President of ETI and was responsible for ETI's sales force.
        ETI distributed transcutaneous electrical nerve stimulator units 
    (TENS units), TENS accessory kits, and lymphedema pumps. Both the TENS 
    unit and the lymphedema pump must be prescribed by a physician in order 
    for Medicare to pay for the equipment. Further, Medicare requires that 
    a physician assess a patient's use of a TENS unit for 30 days prior to 
    authorizing the purchase of the device. In addition, Medicare had very 
    specific diagnoses criteria. If a patient did not have a condition 
    covered by one of these criteria, Medicare would not authorize the 
    purchase of the unit. TENS accessory kits also required a prescription, 
    and were only authorized for distribution every three months.
        Between 1984 and September 1987, ETI billed Medicare $49 million 
    for this equipment, $22 million of which was actually paid to ETI for 
    over 22,000 separate beneficiaries. In an attempt to verify the 
    validity of claims submitted by ETI to Medicare, agents interviewed a 
    number of the Medicare beneficiaries who had received equipment from 
    ETI and physicians whose signatures had served as authorization for the 
    distribution of the medical equipment. The investigation revealed that 
    ETI distributed these units by either sending out sales representatives 
    to ``health fairs'' held at supermarkets, senior citizen centers or 
    banks, or through arrangements with specific geriatric physicians 
    whereby the sales representatives would demonstrate the use of the 
    equipment at the physicians' offices. ETI would then obtain a 
    physicians's signature on a prescription, telling the physician that 
    the patient wanted the equipment.
        However, the patients were told that the equipment was a free gift 
    from Medicare. After learning that Medicare was in fact billed for the 
    equipment, the patients complained because they stated that had they 
    known there would be a charge for the equipment, they would not have 
    accepted it. The investigation
    
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    further revealed that the patients were not assessed for 30 days by a 
    physician before ETI submitted a claim to Medicare for the purchase of 
    the equipment, but that ETI personnel were altering the dates on the 
    prescriptions. It was also determined that ETI personnel were giving 
    patients three to four TENS accessary kits at a time, and altering the 
    dates on the prescriptions that accompanied the Medicare claim forms.
        Given the volume of claims, the agents were unable to investigate 
    the validity of each and every claim. It was determined however, that 
    $3.7 million of the $22 million that was reimbursed by Medicare were 
    false claims that had been altered by ETI personnel. It was the case 
    agent's opinion that 99% of the $22 million in claims were medically 
    unnecessary, as the equipment was provided to patients who did not have 
    a condition that would have caused reimbursement by Medicare.
        Following the investigation, Respondent pled guilty in the United 
    States District Court for the Southern District of New York to one 
    count of conspiracy to make false statements in claims against 
    Medicare, in violation of 18 U.S.C. 371, and to one count of income tax 
    evasion, in violation of 26 U.S.C. 7201. As a result of his conviction, 
    by letter dated December 15, 1994, the Department of Health and Human 
    Services, Office of Inspector General, notified Respondent that he was 
    excluded from participating in the Medicare, Medicaid, Maternal and 
    Child Health Services Block Grant and Block Grants to States for Social 
    Services programs for a period of fifteen years pursuant to 42 U.S.C. 
    1320a-7(a). Subsequently, on May 28, 1996, Respondent and the Inspector 
    General of the Department of Health and Human Services entered into a 
    stipulation, whereby Respondent would be excluded, effective January 4, 
    1995, from participation in the Medicare and Medicaid programs for a 
    period of thirteen years, or until January 4, 2008. In addition, the 
    stipulation included a provision whereby Respondent agreed not to 
    further contest ``now or in the future'' his exclusion from the 
    Medicare and Medicaid programs.
        On October 31, 1995, Respondent entered into a Consent Order with 
    the State of New Jersey, Department of Law and Public Safety, Division 
    of Consumer Affairs, State Board of Medical Examiners (New Jersey 
    Board). The new Jersey Board found that Respondent had engaged in 
    conduct which represented ``crimes of moral turpitude,'' and ordered 
    that Respondent's license to practice medicine and surgery in New 
    Jersey be suspended for 21 months, the first three months to be served 
    as an active suspension, and the remaining 18 months to be served as a 
    period of probation. On May 11, 1995, the Commonwealth of Pennsylvania, 
    Department of State, State Board of Medicine (Pennsylvania Board) and 
    Respondent entered into a Consent Agreement. The Pennsylvania Board 
    ordered, among other things, that Respondent's license to practice 
    medicine and surgery in Pennsylvania be suspended for a period of two 
    years, six months of which to be an active suspension, and the 
    remaining 18 months suspension to be stayed in favor of probation 
    subject to various conditions.
        The Deputy Administrator may revoke or suspend a DEA Certificate of 
    Registration under 21 U.S.C. 824(a), upon a finding that the 
    registrant:
        (1) Has materially falsified any application filed pursuant to or 
    required by this subchapter or subchapter II of this chapter;
        (2) Has been convicted of a felony under this subchapter or 
    subchapter II of this chapter or any other law of the United States, or 
    of any State relating to any substance defined in this subchapter as a 
    controlled substance;
        (3) Has had his State license or registration suspended, revoked, 
    or denied by competent State authority and is no longer authorized by 
    State law to engage in the manufacturing, distribution, or dispensing 
    of controlled substances or has had the suspension, revocation, or 
    denial of his registration recommended by competent State authority;
        (4) Has committed such acts as would render his registration under 
    section 823 of this title inconsistent with the public interest as 
    determined under such section; or
        (5) Has been excluded (or directed to be excluded) from 
    participation in a program pursuant to section 1320a-7(a) of Title 42.
        As noted by Judge Randall, the Order to Show Cause and the 
    statement of the issue agreed to by the parties both alleged that 
    subsections (4) and (5) of 21 U.S.C. 824(a) provide the basis for the 
    revocation of Respondent's DEA Certificates of Registration. However, 
    the Government did not present any evidence nor argue in its post-
    hearing filing that Respondent's continued registration would be 
    inconsistent with public interest pursuant to 21 U.S.C. 824(a)(4). 
    Therefore, the Acting Deputy Administrator agrees with Judge Randall's 
    conclusion ``that the Government has waived the position that a basis 
    for revocation exists under 21 U.S.C. Sec. 824(a)(4) in this matter.'' 
    Consequently, subsection (5) of 21 U.S.C. 824(a) provides the sole 
    basis for the revocation of Respondent's DEA Certificates of 
    Registration.
        Pursuant to 42 U.S.C. 1320a-7(a), Respondent has been excluded from 
    the Medicare and Medicaid programs for 13 years, or until January 4, 
    2008. The Government argues that based upon this exclusion, 
    Respondent's registrations should be revoked. Respondent did not 
    dispute that he has been excluded from the Medicare and Medicaid 
    programs. He did not offer any evidence into the record regarding why 
    his registration should not be revoked. Instead, Respondent argued that 
    the Government had failed to meet its burden of proof that Respondent's 
    continued registration would be inconsistent with the public interest.
        As discussed above, the issue of whether Respondent's continued 
    registration would be inconsistent with the public interest was not 
    pursued by the Government as a basis for revocation. Instead, the 
    Government has presented evidence that Respondent has been excluded 
    from the Medicaid and Medicare programs pursuant to 42 U.S.C. 1320a-
    7(a). Therefore, the Government has met its burden of proving that 
    grounds exist under 21 U.S.C. 824(a)(5) for revoking Respondent's DEA 
    Certificates of Registration. Respondent did not present any evidence 
    as to why his registrations should not be revoked based upon his 
    exclusion from such programs. Respondent did argue that ``DEA had 
    effectually suspended his prescribing privileges, by withholding his 
    renewal, without the benefit of a Court ruling, to the detriment of his 
    patients and their well-being. This constitutes punishment without due 
    process and should be considered by the Court.'' However, as Judge 
    Randall noted, ``the record contains no evidence, such as a denied 
    application for renewal, to support this factual assertion.''
        Judge Randall stated that ``given the lack of rehabilitation 
    evidence, I conclude that circumstances do not exist to deviate from 
    the statutory purpose in this case,'' and recommended that Respondent's 
    DEA Certificates of Registration be revoked. The Acting Deputy 
    Administrator concludes that given the serious nature of the offenses 
    which led to Respondent's convictions, and ultimately to his exclusion 
    from the Medicare and Medicaid programs, and the lack of any evidence 
    of Respondent's rehabilitation or remorse,
    
    [[Page 35529]]
    
    Respondent's registrations should be revoked.
        Accordingly, the Acting Deputy Administrator of the Drug 
    Enforcement Administration, pursuant to the authority vested in him by 
    21 U.S.C. 823 and 824 and 28 CFR 0.100(b) and 0.104, hereby orders that 
    DEA Certificates of Registration BP1786853 and BP2526056, issued to 
    Joseph M. Piacentile, M.D., be, and they hereby are, revoked. The 
    Acting Deputy Administrator further orders that any pending 
    applications for renewal of such registrations, be, and they hereby 
    are, denied. This order is effective July 31, 1997.
    
        Dated: June 24, 1997.
    James S. Milford,
    Acting Deputy Administrator.
    [FR Doc. 97-17152 Filed 6-30-97; 8:45 am]
    BILLING CODE 4410-09-M
    
    
    

Document Information

Published:
07/01/1997
Department:
Drug Enforcement Administration
Entry Type:
Notice
Document Number:
97-17152
Pages:
35527-35529 (3 pages)
Docket Numbers:
Docket No. 96-37
PDF File:
97-17152.pdf