Hobbs Medical, Inc. Hobbs Medical Polypectomy Snare, Catalog No. 7202 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Brand
Hobbs Medical, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
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
Hobbs Medical, Inc. is recalling Hobbs Medical Polypectomy Snare, Catalog No. 7202 due to 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 s. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On June 3, 2022, the firm distributed Urgent Medical Device Recall letters to affected customers. Customers were instructed to immediately cease use of the affected product and to return the product to Hobbs Medical. For questions related to the Acknowledgement Form and its return, please contact Hobbs Customer Service at 1-800-344-6227
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
NC, TX, WA
Page updated: Jan 10, 2026