Reported Jul 27, 2022 · Ongoing
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Hobbs Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hobbs Medical, Inc. · 8 Spring St · Stafford Springs, CT · 06076-1505
Is this the product you have?
- Hobbs Medical Polypectomy Snare, Catalog No. 7202
- Lot codes and dates
- UDI-DIM84972020
- Package UDIM84972021
- Lots
H11-20-017H04-20-062H04-19-056H11-19-077H08-17-014RH10-17-089RH10-17-089H0S-17-014H06-17-167
- Amount recalled
- 45 (US)
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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