Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
Class I - Dangerous 🏥 Medical Devices
Recalled: February 17, 2023 AGILENT TECHNOLOGIES INC./US Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: Model/Part Number: 50032 UDI Code: N/A, single site PMA Lot Numbers: 23-0139 23-0140 23-0142 23-0143 23-0159
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- AGILENT TECHNOLOGIES INC./US
- Reason for Recall:
- Distributed sample collection kit with an unapproved instruction for use.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Agilent Resolution ctDx FIRST Sample Collection Kit, 500032
Product Codes/Lot Numbers:
Model/Part Number: 50032 UDI Code: N/A, single site PMA Lot Numbers: 23-0139 23-0140 23-0142 23-0143 23-0159
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1358-2023