Hobbs Medical Polypectomy Snare — Class II medical device recall Z-1388-2022
Ongoing recall by Hobbs Medical, Inc., reported 2022-07-27, distributed in NC, TX, WA. During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band.
| Recall number | Z-1388-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hobbs Medical, Inc., Stafford Springs, CT, United States |
| Recall initiated | 2022-06-03 |
| Classified | 2022-07-15 |
| Reported by FDA | 2022-07-27 |
| Distributed | NC, TX, WA |
| Countries outside the US | CA |
| Quantity | 45 |
| Lot numbers | H04-19-056, H04-20-062, H06-17-167, H08-17-014R, H0S-17-014, H10-17-089, H10-17-089R, H11-19-077, H11-20-017 |
| Model numbers | 7202 |
Product
Hobbs Medical Polypectomy Snare, Catalog No. 7202
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1388-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.