Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lase DiscectomLase Discectomy Device Kit Recalled by Clarus Medical, Llc Due to The sterile barrier seal may be compromised.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Clarus Medical, Llc directly.
Affected Products
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Quantity: 858 units
Why Was This Recalled?
The sterile barrier seal may be compromised.
Where Was This Sold?
Distribution in US - 18 accounts 1 foreign account
About Clarus Medical, Llc
Clarus Medical, Llc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report