Class II — Hobbs Medical, Inc.
| Recalling firm | Hobbs Medical Inc |
|---|---|
| Registered facility | HOBBS MEDICAL, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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 |
| Quantity | 45 (US) |
| Distribution | Domestic distribution to NC, TX, and WA. Foreign distribution to Canada. |
| Initiated | 2022-06-03 |
| Classified | 2022-07-15 |
| Recall number | Z-1388-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Hobbs Medical, Inc. (Z-1388-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90456/
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