Reported Dec 23, 2020 · Ongoing
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE…
Helena Laboratories, Corp.
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: Helena Laboratories, Corp. · 1530 Lindbergh Dr · Beaumont, TX · 77707-4131
Is this the product you have?
- K-ACT Actalyke Clotting
- Test Tubes that are used in theACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM
- Lot codes and dates
- Catalog NumberK-ACT
- Lot Number1-19-K-ACT and 2-19-K-ACT
- Amount recalled
- Lot 1-19-K-ACT = 314 tubes and Lot 2-19-K-ACT = 297 tubes
Where it was sold
Why it was recalled
Due to complaints received associated with cracked/split test tube caps.
This product could cause temporary or reversible health problems — stop using it.
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