Hobbs Medical, Inc.: Medical Device Recall in 2022 - (Recall #: Z-1388-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Hobbs Medical Polypectomy Snare, Catalog No. 7202

Product Classification:

Class II

Date Initiated: June 3, 2022

Date Posted: July 27, 2022

Recall Number: Z-1388-2022

Event ID: 90456

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.

Status: Ongoing

Product Quantity: 45 (US)

Code Information:

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

Distribution Pattern:

Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.

Voluntary or Mandated:

Voluntary: Firm initiated