Hobbs Medical Polypectomy Snare, Catalog No. 7202
Reported: July 27, 2022 Initiated: June 3, 2022 #Z-1388-2022
Product Description
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.
Details
- Recalling Firm
- Hobbs Medical, Inc.
- Units Affected
- 45 (US)
- Distribution
- Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.
- Location
- Stafford Springs, CT
Frequently Asked Questions
What product was recalled? ▼
Hobbs Medical Polypectomy Snare, Catalog No. 7202. Recalled by Hobbs Medical, Inc.. Units affected: 45 (US).
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 27, 2022. Severity: Moderate. Recall number: Z-1388-2022.
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