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Intersect ENT, Inc.

Intersect ENT, Inc. Recalls

All product recalls associated with Intersect ENT, Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Jan 2023

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–2 of 2 recalls

SINUVA Sinus Implant (Intersect ENT) – Failed Dissolution (2023)

Failed Dissolution Specification; product did not meet the average 24-hour drug release rate (dissolution) specification stability time point at 9 months.

Class IIILow

FDAJan 4, 2023Nationwide• Intersect ENT, Inc.

Propel Mini Sinus Implant (Intersect ENT) – Label Error (2022)

Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI.

Moderate

FDAOct 21, 2022Nationwide• Intersect ENT, Inc.