FDAJune 3, 2022device

Hobbs Medical Polypectomy Snare, Catalog No. 7202

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

The hazard

During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the snare from fully closing, and injury may result.

What to do

FDA enforcement status: Ongoing

Brands named

hobbs medicalhobbs

Recall history

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

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Hobbs Medical Polypectomy Snare, Catalog No. 7202 — Recall Details · AllClear