Instrumentation Laboratory recalls HemosIL ReadiPlasTin, Part No. 0020301400
Variable and out of specification QC results with HemosIL ReadiPlasTin. IL will remove all lots from the market and convert customers to an alternative prothrombin time (PT) reagent, specifically HemosIL RecombiPlasTin…
Read the official notice →- Date
- 2022-05-18
- Country
- United States
- Brand
- Instrumentation Laboratory
- Product
- HemosIL ReadiPlasTin, Part No. 0020301400
- Classification
- Class II
- Units
- US Nationwide distribution including in the states of AZ, CA, IA, IL, IN, KS,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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