Clarus Medical, Llc recalls Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
- Recall date
- July 27, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2405-2021
- FDA classification
- Class II
- Brand / firm
- Clarus Medical, Llc
- Sold / distributed
- Distribution in US - 18 accounts 1 foreign account
Why it was recalled
The sterile barrier seal may be compromised.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
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