FDA device recall (Class II): Clarity II Laser System; Model No. 1110200210.
FDA recalls Clarity II Laser System for safety concerns.
What changed & why it matters
Med Spa Radar recorded an FDA device recall at the federal level, dated March 18, 2026, in the Aesthetic Devices category.
A recall is a supply-chain event, not a rule that might change: if the pharmacy or outsourcing facility a med spa sources from distributed an affected lot, it is a patient-safety and liability exposure today. Recalls are the clearest signal that a supplier a practice may already use has a quality problem on record with the FDA.
- Type
- FDA Device Recall
- Jurisdiction
- Federal
- Category
- Aesthetic Devices
- Recorded
- March 18, 2026
What this means for your specific practice — the exact step to take, the deadline to calendar, or the supplier detail to check — is in the member "what to do" below. This page is the free record of what changed and why it matters.
What to do
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FDA Device Recall · primary source ↗
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Monitoring, not legal advice.