Reported Sep 8, 2021 · Terminated
Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
Clarus Medical, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Clarus Medical, Llc · 13355 10th Ave N Ste 110 · Minneapolis, MN · 55441-5554
Is this the product you have?
- Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002
- Lot codes and dates
Model Numbers 1100-002 and 1100-002 SHORTSerial Numbers 64139 through 65022
- Amount recalled
- 858 units
Why it was recalled
The sterile barrier seal may be compromised.
This product could cause temporary or reversible health problems — stop using it.
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