🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: October 21, 2022 Intersect ENT Implants & Prosthetics Nationwide

What Should You Do?

  1. Check if you have this product:
    REF: 60044, UDI-DI: M927600440, Lot: 22041901
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Intersect ENT, Inc.
Reason for Recall:
Sinus Implant product label displays incorrect product information including: "Straight Delivery System", with incorrect reference number and UDI-DI.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

REF: 60044, UDI-DI: M927600440, Lot: 22041901

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0458-2023

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