🔍 RecallPedia

Solero Generator Refurbished PG, Item No. H78712740000D0, Catalog No. 12740000D

Class I - Dangerous
🏥 Medical Devices Recalled: July 20, 2021 Angiodynamics Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Serial Nos. QBY0002816 QBY0002817 QBY0002348 QBY0002308 QBY0002311 QBY0002711 QBY0002741 QBY0002858
  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:
Angiodynamics, Inc.
Reason for Recall:
Specific serial numbers of the Solero MTA Generator require servicing to upgrade the software to help reduce the incidence of Error 0001, which can occur during system start-up.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Solero Generator Refurbished PG, Item No. H78712740000D0, Catalog No. 12740000D

Product Codes/Lot Numbers:

Serial Nos. QBY0002816 QBY0002817 QBY0002348 QBY0002308 QBY0002311 QBY0002711 QBY0002741 QBY0002858

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2438-2021

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