🇺🇸·Sep 9Regulatory
Device recall: LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS US, Model Number 7260, All Versions (Current 7.8)
Official structured record identifier: 99524.
Publisher
o
openFDA Device Recalls
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- September 9, 2026
- Language
- EN
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Official structured record identifier: 99524.
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Source: openFDA Device Recalls
Scope: Regulatory
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