QuidelOrtho (QDEL) Q3 2024 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2024 earnings summary
8 Jul, 2026Executive summary
Q3 2024 revenue was $727 million, down 2% year-over-year, with recurring revenue at $598 million and Labs recurring revenue up 6% in constant currency.
Adjusted EBITDA for Q3 was $171 million (23.5% margin), and adjusted diluted EPS was $0.85, reflecting margin improvement from cost-saving and operational initiatives.
Leadership changes included new CTO and CHRO, and a flatter organizational structure to enhance efficiency and customer focus.
A non-cash goodwill impairment charge of $1.7 billion was recorded for the North America reporting unit, driving a net loss of $1.87 billion for the nine months ended September 29, 2024.
The company reinstated full-year 2024 guidance, projecting total revenue of $2.75–$2.80 billion, adjusted EBITDA of $530–$550 million, and adjusted diluted EPS of $1.69–$1.91.
Financial highlights
Q3 adjusted EBITDA was $171 million (23.5% margin), up 80 basis points year-over-year; adjusted diluted EPS was $0.85, down from $0.90 prior year.
Q3 adjusted gross profit margin was 49.2%, down 130 basis points from the prior year, mainly due to product mix.
Q3 GAAP net loss was $20 million, with a net loss margin of (3%) and GAAP operating margin of 2%.
Adjusted free cash flow in Q3 was $120 million, representing 70% of adjusted EBITDA.
YTD 2024 revenue was $2.08 billion, down 7% year-over-year; recurring revenue grew 5% to $1.74 billion.
Outlook and guidance
Full-year 2024 revenue expected at $2.75–$2.80 billion, adjusted EBITDA $530–$550 million, and adjusted diluted EPS $1.69–$1.91.
2024 COVID-19 revenue projected at $160–$170 million; Labs and transfusion medicine (excluding U.S. Donor Screening) expected to grow mid- and low-single digits, respectively.
2025 outlook anticipates mid-single digit top-line growth (excluding COVID-19 and U.S. Donor Screening), with further margin improvement of 100–200 basis points.
The wind-down of the U.S. donor screening portfolio is expected to be substantially complete by the end of 2025.
The company anticipates sufficient liquidity to fund near-term capital and operating needs for at least the next 12 months.
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