FDA Device recall Z-1388-2022
Hobbs Medical Polypectomy Snare, Catalog No. 7202
- FDA Device
- Class II
- ongoing
- Published 2022-07-27
On 2022-07-27 the FDA classified a Class II recall of Hobbs Medical Polypectomy Snare, Catalog No. 7202 by Hobbs Medical, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1388-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-06-03 |
| Published | 2022-07-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Hobbs Medical |
| Distribution | NC, TX, WA |
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.
Identifiers
| code_info | 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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1388-2022%22
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