Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hobbs Medical Polypectomy Snare Recalled by Hobbs Medical, Inc. Due to During use, the sheath of the device may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hobbs Medical, Inc. directly.
Affected Products
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Quantity: 45 (US)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 3 states: NC, TX, WA
About Hobbs Medical, Inc.
Hobbs Medical, Inc. has 73 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report