Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.
Class I - Dangerous 🏥 Medical Devices
Recalled: August 10, 2022 Steris Corporation Hopkins Facility Diagnostic Equipment
Nationwide
What Should You Do?
- Check if you have this product: UDI-DI (GTIN): 10724995088955 Item Number: LCC003, Lot 3411228A
- 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:
- Steris Corporation Hopkins Facility
- Reason for Recall:
- Product contains incorrect chemical indicators in packaging.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within a challenging test pack design.
Product Codes/Lot Numbers:
UDI-DI (GTIN): 10724995088955 Item Number: LCC003, Lot 3411228A
Distribution:
Nationwide distribution
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1736-2022