Drug recall
Hobbs Medical Polypectomy Snare, Catalog No. 7202
FDA recall event 90456 · Class II · Hobbs Medical, Inc.
Key facts
| Event ID | 90456 |
|---|---|
| Recall numbers | Z-1388-2022 |
| Recalling firm | Hobbs Medical, Inc. |
| Product type | Devices |
| Products | Hobbs Medical Polypectomy Snare, Catalog No. 7202 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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. |
| Initiation date | Jun 3, 2022 |
| Report date | Jul 27, 2022 |
| City | Stafford Springs |
| State | CT |
| Country | United States |
| FEI number | 1220592 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: