Beckman Coulter recalls remanufactured Access 2 Immunoassay System (Catalog 386220) with serial numbers 507114, 503299, 508111 due to potential minor skin burns from reagent storage interface board contact during pipettor alignment.
Potential for minor skin burn if the tool contacts the reagent storage interface board (B79917) when performing a pipettor alignment.
Beckman Coulter is recalling remanufactured Access 2 Immunoassay Systems with specific serial numbers because they could cause minor skin burns if the pipettor aligns with the reagent storage interface board. This is a minor hazard that doesn't require immediate stoppage but should be addressed to prevent skin irritation.
The device's reagent storage interface board (B79917) could cause minor skin burns if the pipettor aligns with it during use. This happens when the tool contacts the board during pipettor alignment procedures, which is a minor skin irritation risk but not life-threatening.
Users of the remanufactured Access 2 Immunoassay System with serial numbers 507114, 503299, or 508111 are affected. Laboratory technicians and medical professionals using this device for in vitro diagnostics are most at risk.
Check for the Access 2 Immunoassay System with remanufactured status and catalog number 386220. The affected units have serial numbers 507114, 503299, or 508111.
If you experience skin irritation after using the device, stop use immediately and contact Beckman Coulter for assistance.
Confirm your device's serial number matches the affected numbers: 507114, 503299, or 508111.
No, the recall involves a potential for minor skin burns, not serious injury or death.
Check if your Access 2 Immunoassay System has serial numbers 507114, 503299, or 508111.
No, but if you experience skin irritation, stop use and contact Beckman Coulter.
We’ve drafted a message you can send Beckman Coul: Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0309-2018 — Beckman Coul: Inc. Beckman Coul: Inc. Hello, I own a Beckman Coul: Inc. that is covered by recall Z-0309-2018 from Beckman Coul: Inc.. 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.
