Medical Device Intelligence, Always Current
Independent, sourced intelligence on global medical device regulation, product recalls and the companies shaping the industry.
FDA's updated provider letter lists five models under an October 20, 2026 heading, while preserving qualified use of existing equipment and exclusions for related supplies. Import restrictions remain product- and facility-specific.
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Published
Published
Recall Brief Class I
Nova Biomedical Corporation ·
Recall Brief Class I
Philips Ultrasound, LLC ·
Recall Brief Class I
BD SWITZERLAND SARL (Z-3080-2026); CareFusion 303, Inc. (linked earlier actions) ·
Sourced analysis of global medical device regulatory developments.
Concise briefs connecting official notices to products and manufacturers.
Companies, competitive movements and the sectors shaping MedTech.
Coming soonTools that turn trusted intelligence into comparisons and visuals.
In development