BOSTON SCIENTIFIC CORP quarterly report, Q2 FY2018

Boston Scientific Corporation — Q2 2018 Form 10-Q

Reporting period: Three and six months ended June 30, 2018. Amounts are in U.S. dollars; financial statement amounts are in millions unless stated otherwise. Boston Scientific develops and sells medical devices across cardiovascular, digestive, respiratory, urological, pelvic health and neurological markets.

Financial performance

MetricQ2 2018Q2 2017Six months 2018Six months 2017
Net sales$2,490$2,257$4,870$4,418
GAAP gross profit$1,751$1,625$3,458$3,136
GAAP gross margin70.3%72.0%71.0%71.0%
GAAP operating income$392$225$799$589
GAAP net income$555$146$853$436
Diluted GAAP EPS$0.40$0.11$0.61$0.31
Cash from operating activitiesNot separately stated for Q2$(210)$290
  • Reported sales grew 10.3% in Q2 and 10.2% in the first half. On a constant-currency operational basis, growth was 8.6% and 7.4%, respectively; currency contributed 170 and 280 basis points to reported growth.
  • Management’s non-GAAP adjusted net income was $568 million, or $0.41 per diluted share, in Q2 versus $444 million, or $0.32, a year earlier. First-half adjusted net income was $1.023 billion, or $0.73 per diluted share, versus $841 million, or $0.60.
  • Q2 gross margin declined 1.7 percentage points year over year, chiefly from foreign-currency effects, partly offset by manufacturing cost reductions. First-half gross margin was unchanged. SG&A declined as a share of sales; R&D spending rose in dollars and remained about 11% of sales.
  • First-half operating cash flow turned negative, primarily because of the IRS tax settlement. Investing cash outflow was $664 million, including $418 million for acquisitions and $112 million for strategic investments and technology acquisitions. Financing provided $856 million.

Balance sheet and liquidity

  • At June 30, cash and cash equivalents were $208 million; this excludes $787 million of restricted cash and restricted cash equivalents. Total cash, cash equivalents and restricted cash was $994 million.
  • Total debt was $6.493 billion, up from $5.616 billion at December 31, 2017. Debt included $1.685 billion of commercial paper and $4.808 billion of long-term debt. The company issued $1.0 billion of 4.0% notes due 2028 and used proceeds in part to repay $600 million of notes due in 2018 and reduce commercial paper.
  • Working capital was negative $825 million. The company reported $565 million of remaining commercial-paper capacity under its $2.25 billion program and $400 million available under its receivables-backed facility. No amounts were drawn on either revolving/receivables facility at quarter-end.
  • The leverage covenant maximum was 3.5x; the reported ratio was 2.4x. The company stated it was in compliance with debt covenants and expected available cash, operating cash generation, capital-market access and credit facilities to fund needs for the next 12 months.

Material changes and business developments

  • Q2 revenue growth was broad-based: operational sales rose 9.0% in MedSurg, 9.0% in Rhythm and Neuro, and 8.0% in Cardiovascular. Neuromodulation grew 30.6% operationally; Cardiac Rhythm Management grew 1.2%.
  • Emerging-market Q2 sales rose 21.1% operationally. The company reorganized reporting segments effective January 1, 2018, moving Neuromodulation from MedSurg into the new Rhythm and Neuro segment; prior segment comparisons were recast.
  • Acquisitions completed in the first half included NxThera and nVision. The company also invested $90 million in Millipede. After quarter-end, it closed the Cryterion acquisition for $202 million and announced an agreement to acquire Claret Medical for $220 million upfront plus potential milestones.
  • Adoption of the new revenue standard reduced opening retained earnings by $177 million, primarily for estimated post-implant support costs. The standard also resulted in accrued support liabilities. Other reported adoption impacts were not material.

Outlook, unusual items and risks

  • No specific company sales or earnings guidance is provided in the supplied filing text. Management expects the 2016 restructuring plan to produce $165–$175 million of annual gross expense reductions by the end of 2020, with a substantial portion reinvested in growth initiatives. Estimated total plan charges are $275–$325 million; completion is expected by the end of 2018.
  • Q2 GAAP net income included a net tax benefit from resolution of IRS disputes; the company reported a $250 million net tax benefit related to the settlements. It paid the IRS $303 million in tax plus $307 million of estimated interest. The settlement and other discrete tax items materially affect comparisons of reported earnings and cash flow.
  • The first-half effective tax rate was negative 27.3%, versus negative 10.1% in 2017, reflecting unusual tax items, including the IRS settlement and Tax Cuts and Jobs Act estimates. Management said it expected to resolve the 2011–2013 IRS examination before year-end 2018 and believed reserves were sufficient.
  • Legal reserves were $1.264 billion at June 30. Approximately 49,500 transvaginal mesh cases or claims had been asserted; settlement agreements in principle or final-stage agreements covered approximately 48,000, of which approximately 27,000 were final. Further losses could be accrued, and the outcome could materially affect results, cash flows or liquidity.
  • Other principal risks include product liability and patent litigation, regulatory and governmental investigations, product quality and approval requirements, reimbursement and pricing pressure, foreign-exchange exposure, acquisition integration and contingent payments, and the ability to maintain cash generation and covenant compliance. Maximum potential future contingent consideration was approximately $1.532 billion, undiscounted.

Important facts for investors to verify

  • Separate underlying operating growth from currency effects and acquisition contributions; assess whether strong segment growth is sustained.
  • Reconcile reported earnings to adjusted earnings, especially the IRS settlement, tax benefits, amortization, impairment, acquisition and restructuring adjustments.
  • Track operating cash conversion after the settlement-related outflow, the working-capital deficit, commercial-paper refinancing needs and debt levels.
  • Monitor mesh litigation settlements, legal reserves and potential additional claims, together with remaining tax examinations.
  • Evaluate acquisition integration, milestone obligations and the execution and realized savings of the restructuring plan.