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Clarus Medical, Llc recalls Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Recalled September 8, 2021 · FDA recall Z-2405-2021 · Clarus Medical
Hazard
The sterile barrier seal may be compromised. · FDA Class II
Units
858 units
Sold at
Distribution in US - 18 accounts 1 foreign account
Description
The sterile barrier seal may be compromised.
Product
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Manufacturer(s)
Clarus Medical, Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →