Helena Laboratories, Corp. recalls K-ACT Actalyke Clotting Test Tubes that are used in the: ACT
Recalled Product
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE MINI ACTIVATED CLOTTING TIME TEST SYSTEM.
Hazard / Issue
Due to complaints received associated with cracked/split test tube caps.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Catalog Number: K-ACT Lot Number: 1-19-K-ACT and 2-19-K-ACT
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime