Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hemosll ReadiPlasTin (20 ml Size) Recalled by Instrumentation Laboratory Co. Due to Instrumentation Laboratory Co. received customer reports of performance...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Instrumentation Laboratory Co. directly.
Affected Products
Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400
Quantity: 14,894 kits
Why Was This Recalled?
Instrumentation Laboratory Co. received customer reports of performance issues with some vials of Lot Nos. N1166235 and N0177760, including increased imprecision, out of range quality controls and prolonged sample results.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Instrumentation Laboratory Co.
Instrumentation Laboratory Co. has 31 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report