Recall archive / FDA device enforcement
Hobbs Medical Polypectomy Snare, Catalog No. 7202 — FDA record Z-1388-2022
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jun 3, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Hobbs Medical Polypectomy Snare, Catalog No. 7202
- 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.
- Classification
- Class II
- Recalling firm
- Hobbs Medical, Inc.
- Quantity
- 45 (US)
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1388-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: M84972020 Package UDI: M84972021 Lots: H11-20-017 H04-20-062 H04-19-056 H11-19-077 H08-17-014R H10-17-089R H10-17-089 H0S-17-014 H06-17-167 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jul 27, 2022
- Recall initiation date
- Jun 3, 2022
- Center classification date
- Jul 15, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.