FDAJuly 27, 2021device

Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The sterile barrier seal may be compromised.

What to do

FDA enforcement status: Terminated

Brands named

clarus medicalclarus

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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