FDAOctober 21, 2022device

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044 — Recall Details · AllClear