Thank you, Melinda, and good morning, everyone. It is my pleasure to welcome you to STERIS’s Fiscal 2013 Second Quarter Conference Call. Thank you for taking the time to join us this morning. With me today is Walt Rosebrough, our President and CEO.
Now just a few words of caution before we begin. This webcast contains time-sensitive information that is accurate only as of today, October 31, 2012. Any redistribution, retransmission or rebroadcast of this call without the expressed written consent of STERIS is strictly prohibited.
I would also like to remind you that the discussion may contain forward-looking statements related to the company, its performance or its industry which are intended to qualify it for the protection under the Private Securities Litigation Reform Act of 1995. No assurance can be given as to any future financial results. Actual results could differ materially from those in the forward-looking statements. The company does not undertake to update or revise these forward-looking statements, even as events make it clear that any projected results expressed or implied in this or company statements will not be realized.
Investors are further cautioned not to place undue reliance on any forward-looking statements. Statements involve risks and uncertainties, many of which are beyond the company’s control. Additional information concerning factors which could cause actual results to differ materially is contained in today’s earnings release. As a reminder, during the call we may refer to non-GAAP measures, such as adjusted earnings, free cash flow, backlog, debt-to-total capital, days sales outstanding, all of which are defined and reconciled, as appropriate, in today’s press release or our most recent 10-K filing, both of which can be found at steris-ir.com.
As you saw this morning in our earnings announcements, during the quarter, we reversed a portion of our original SYSTEM 1 Rebate Program liability. The total pre-tax reversal was $21.5 million and is based on actual experience to date. Of the total reversal, $20.4 million is attributable to the Customer Rebate portion of the program and was recorded as an increase to revenue and the remaining $1.1 million is attributable to the disposal costs related to SYSTEM 1 units to be returned and was recorded as a reduction to cost of revenue.
In addition, in the quarter, we incurred a total of $5 million or $0.06 per diluted share of costs related to the recent acquisitions of U.S. Endoscopy, Total Repair services and Spectrum.
I want to highlight that many of the comments made today by Walt and me are based on adjusted or non-GAAP measures. I also want to point out that starting this quarter, our fiscal 2013 guidance will now be provided solely on an adjusted basis. That means that revenue, net income and earnings per diluted share will exclude the impact of the SYSTEM 1 Rebate Program reversal, amortization of purchased intangible assets, acquisition-related transaction and integration costs, as well as certain other items.
We believe that the adjusted measurements provide meaningful information in order to assist investors and shareholders in understanding our financial results and in assessing future performance. Reconciliations to our reported U.S. GAAP numbers are included in today’s earnings release.
With that I will now begin with a review of our second quarter income statement.
Total revenue declined 2% during the second quarter, driven by a 5% decline in volume and a 1% negative impact from currency fluctuations, offset by a 3% increase from acquisitions and a 1% improvement in pricing. Gross margin in the quarter increased 30 basis points to 39.4%. While we are pleased with this improvement, we continue to be negatively impacted from our U.S. SYSTEM 1 and 1E business on the gross margin line. The rest of our business, excluding SYSTEM 1 and 1E, expanded gross margin by 120 basis points, reflecting the benefits of product mix and favorable foreign currency fluctuations.
EBIT for the quarter decreased $2.6 million to $47.2 million. EBIT as a percentage of revenue for the quarter was 14%, a decrease of 50 basis points from last year, caused by lower revenue attainment. Net income for the quarter was $31 million or $0.53 per diluted share, the same as the prior-year second quarter.
Moving on to our segments results. Healthcare revenue in the quarter declined 3%. Capital equipment revenue declined 11%, driven by the expected post-transition decline in SYSTEM 1E unit sales and some international weakness, offset by growth in the United States. Consumable revenue increased 12%, as growth in other consumables more than offset continued reductions in the combined S20/S40 sterilant volumes.
Service revenue increased 2%, driven primarily by growth in service contracts. Healthcare revenue in the quarter - sorry, Healthcare backlog in the quarter was $119.2 million. Given where we are in the SYSTEM 1 transition process, our SYSTEM 1E backlog, as anticipated, has been substantially eliminated. Healthcare backlog, excluding SYSTEM 1E, is lower by 9% versus the prior year, but has increased 21% sequentially.
Healthcare operating margin in the quarter was 11.3% of revenue. This represents a decline versus the prior year, caused by lower revenue attainment due to the timing of shipments, the phase out of S20 sterilant in the U.S. and fewer SYSTEM 1E units.
Life Sciences revenue decreased 7% in the quarter. Capital equipment revenue declined 24%. Consumables revenue grew 5% and service revenue grew 1%. Backlog in Life Sciences was $50.6 million at the end of the quarter, an increase of 23% compared with last year. Life Sciences operating margin increased to 19.3%. The operating margin expansion is a result of a mix shift towards recurring revenue in the quarter.
Revenue for Isomedix increased 11% in the quarter. We continue to experience solid demand from our core medical device customers, as well as a positive impact from our acquisition of Biotest. Isomedix's operating margin increased by 60 basis points as a result of increases in revenue volume. In terms of the balance sheet, we ended the quarter with $156.6 million of cash, the bulk of which sits outside of the United States and $434.3 million in long-term debt.
Our long-term debt consists of $210 million from our private placement funding and $224 million drawn from our revolving credit facility used to partially fund the acquisition of U.S. Endoscopy. Our total debt-to-capital ratio is 33.1% and our total net debt-to-total capital ratio is 24%. Our free cash flow for the first half of fiscal 2013 was $67 million compared with $26.1 million in the prior year.
We continue to make good progress on improving our working capital position both sequentially and year-over-year. The improvement in free cash flow is attributable to reductions in inventory levels, lower DSOs and less cash required to fund compensation-related obligations.
Our inventory levels, as anticipated, have been substantially reduced as compared to the prior year.
The reduction of over $20 million in SYSTEM 1E-related inventory, driven by shipments of SYSTEM 1E units, contributed significantly to the reduction. In addition, our DSO now at 60 days, has improved by 3 days as compared to the prior year. Capital spending was $29.5 million in the quarter, while depreciation and amortization was $15.9 million.
With that, I will now turn the call over to Walt for his remarks. Walt?