🔍 RecallPedia

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Class I - Dangerous
🏥 Medical Devices Recalled: April 30, 2026 Avanos Medical Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746
  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:
Avanos Medical, Inc.
Reason for Recall:
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No

Product Codes/Lot Numbers:

Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2342-2026

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