🔍 RecallPedia

DiamondTOUCH Digital Inflation Device, REF: IN9135/A, IN9152/A

Class I - Dangerous
🏥 Medical Devices Recalled: August 19, 2024 Merit Medical Systems Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    REF/UDI-DI/Lot(Expiration): IN9135/A/00884450409640/H2918441(4/15/2027). IN9152/A/00884450409657/H2912682(4/8/2027)
  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:
Merit Medical Systems, Inc.
Reason for Recall:
Inflation devices may have a small hole in the sterile barrier of the device and use of affected devices may result in exposure to pathogens/pyrogens which could lead to infection.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

DiamondTOUCH Digital Inflation Device, REF: IN9135/A, IN9152/A

Product Codes/Lot Numbers:

REF/UDI-DI/Lot(Expiration): IN9135/A/00884450409640/H2918441(4/15/2027). IN9152/A/00884450409657/H2912682(4/8/2027)

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0066-2025

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