Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot 50083Y600, expiration date 31 Jul 2016.
- 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:
- Sentinel CH SpA
- Reason for Recall:
- Results for ammonia are below the linear range of the assay for samples that have been collected in sodium or lithium heparin tubes.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma.
Product Codes/Lot Numbers:
Lot 50083Y600, expiration date 31 Jul 2016.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0164-2016
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