Clarus Medical, Llc Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Brand
Clarus Medical, Llc
Lot Codes / Batch Numbers
Model Numbers 1100-002 and 1100-002 SHORT, Serial Numbers 64139 through 65022
Products Sold
Model Numbers 1100-002 and 1100-002 SHORT; Serial Numbers 64139 through 65022
Clarus Medical, Llc is recalling Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 110 due to The sterile barrier seal may be compromised.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The sterile barrier seal may be compromised.
Recommended Action
Per FDA guidance
The affected Domestic customers, Domestic/International Distributors will be notified with a Field Safety Notice. Domestic/International distributors will also include a request for a list of the Distributor s customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026