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Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare, Catalog No. 7202
Recalled July 27, 2022 · FDA recall Z-1388-2022 · Hobbs Medical
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. · FDA Class II
Units
45 (US)
Sold at
Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.
Description
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.
Product
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Manufacturer(s)
Hobbs Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →