Reported Nov 4, 2015 · Terminated
Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement; List Number: LN 6K89-30.…
Sentinel CH SpA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Sentinel CH SpA · Via Robert Koch 2 · Milano, N/A · N/A
Is this the product you have?
- Sentinel MULTIGENT Ammonia Ultra Reagent, In-Vitro Diagnostic for ammonia measurement
- List NumberLN 6K89-30. Intended for the in vitro quantitative determination of Ammonia (NH3) in human plasma
- Lot codes and dates
Lot 50083Y600expiration date 31 Jul 2016
- Amount recalled
- 765 kits
Where it was sold
- Nationwide
Why it was recalled
Results for ammonia are below the linear range of the assay for samples that have been collected in sodium or lithium heparin tubes.
This product could cause temporary or reversible health problems — stop using it.
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