Clarus Medical, Llc recalls Lase DiscectomLase Discectomy Device Kit, Models 1100-002 an
Recalled Product
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Hazard / Issue
The sterile barrier seal may be compromised.
Issued by
FDA
Distribution: Distribution in US - 18 accounts 1 foreign account
Lot/Code Info: Model Numbers 1100-002 and 1100-002 SHORT; Serial Numbers 64139 through 65022
View official government recall
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