Hobbs Medical recalls polypectomy snare (Catalog No. 7202) due to sheath kinking risk during use, which may cause injury. Affected units include specific lots and package UDI codes.
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.
Hobbs Medical is recalling polypectomy snare devices with catalog number 7202 because the sheath can kink during use, potentially preventing the snare from closing and causing injury. This recall affects medical devices used in procedures to remove polyps.
The sheath of the device can accordion at the proximal end where it meets the shrink band. This kinking may prevent the snare from fully closing, which could lead to injury during medical procedures.
Healthcare professionals who use the Hobbs Medical Polypectomy Snare (Catalog No. 7202) are most at risk. Patients undergoing procedures with this device may also be affected.
Check for the catalog number 7202 on the device. Affected units include specific 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.
Look for the lot numbers listed in the recall: 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.
The catalog number is 7202.
Affected lot numbers include H11-20-017, H04-20-062, H04-19-056, H11-19-077, H08-17-014R, H10-17-089R, H10-17-089, H0S-17-014, and H06-17-167.
The recall record does not specify a remedy.
We’ve drafted a message you can send Hobbs Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1388-2022 — Hobbs Medical Hobbs Medical Hello, I own a Hobbs Medical that is covered by recall Z-1388-2022 from Hobbs Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.