Bio-Rad recalls PR4100 Microplate Readers with specific serial numbers due to power supply connector incompatibility that could cause system damage if incorrectly connected.
The connector of the power supply was capable of fitting other components provided with the system. However, the voltage output of the reader power supply is incompatible with the other component and, if incorrectly connected, could result in irreparable damage to the system.
Bio-Rad is recalling certain PR4100 Microplate Readers because their power supply connector might fit other components, but the voltage output is incompatible. This could cause irreparable damage to the system if incorrectly connected.
The power supply connector can fit other components, but the voltage output is incompatible with those components. If incorrectly connected, this could cause irreparable damage to the system without causing injury or harm to the user.
Users of the PR4100 Microplate Reader with specific serial numbers listed in the recall notice. Laboratory technicians and researchers using this equipment are most at risk.
Check if your PR4100 Microplate Reader has a serial number listed in the provided list (e.g., 140600072, 160900991, etc.). The product is a 96-well absorbance reader for laboratory use.
Verify your PR4100 Microplate Reader's serial number against the list provided in the recall notice.
The power supply connector can fit other components, but the voltage output is incompatible with those components. If incorrectly connected, this could cause irreparable damage to the system.
Check your serial number against the list provided in the recall notice. If it's listed, you may need to contact Bio-Rad for further instructions.
No, the hazard only risks irreparable damage to the system, not injury or harm to users.
We’ve drafted a message you can send Bio-Rad to request your refund or repair — edit it as you like.
Subject: Recall Z-2541-2018 — Bio-Rad Bio-Rad Hello, I own a Bio-Rad that is covered by recall Z-2541-2018 from Bio-Rad. 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.
