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.
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.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Instrumentation Laboratory Co. to request your refund or repair — edit it as you like.
Subject: Recall Z-0895-2018 — Instrumentation Laboratory Co. Instrumentation Laboratory Co. recalls Hemosll ReadiPlasTin (20 ml S Hello, I own a Instrumentation Laboratory Co. recalls Hemosll ReadiPlasTin (20 ml Size), Part Number 0020301400 that is covered by recall Z-0895-2018 from Instrumentation Laboratory Co.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
