Alcor Scientific recalls iSED Primary Pump Tubing Spare Part Kit (PN 112-13-002, Lot 4/2: potential biohazard leak if installed on iSED ESR Analyzer.
Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto an ALCOR iSED ESR Analyzer, there is a potential of a biohazard leak from the iSEDs Probe Tube
Alcor Scientific is recalling a spare part kit for their iSED ESR Analyzer. The tubing may cause a biohazard leak if installed incorrectly, which could expose users to harmful biological materials.
The tubing is incorrect and may cause a biohazard leak from the analyzer's probe tube if installed. This could expose users to harmful biological materials during sample testing.
Users of Alcor iSED ESR Analyzers who have the spare tubing kit (PN 112-13-002, Lot 4/22) are affected. Lab technicians and medical personnel using the analyzer are at highest risk.
Check for the part number PN 112-13-002 and lot number 4/22 on the tubing kit. The tubing is used with Alcor iSED ESR Analyzers to move samples and wash solutions.
Verify the part number and lot number on the tubing kit to ensure it matches PN 112-13-002 and Lot 4/22.
The tubing is incorrect and may cause a biohazard leak from the iSED ESR Analyzer's probe tube if installed, potentially exposing users to harmful biological materials.
Check the part number and lot number to confirm it matches PN 112-13-002 and Lot 4/22. If it does, contact Alcor Scientific for a replacement.
The recall states a potential biohazard leak, but no specific mention of serious injury. The hazard is considered low risk for serious injury.
We’ve drafted a message you can send Alcor Scientific to request your refund or repair — edit it as you like.
Subject: Recall Z-1751-2022 — Alcor Scientific Alcor Scientific Hello, I own a Alcor Scientific that is covered by recall Z-1751-2022 from Alcor Scientific. 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.
