Magellan recalls LeadCare Plus blood lead analyzers with specific battery boards due to risk of battery overheating and finger burns if removed while hot.
The incorrect placement of AA batteries into certain LeadCare Plus Blood Lead Analyzer may cause the batteries to overheat, and the chance that a user could burn their fingers if the batteries are removed while hot.
Magellan is recalling LeadCare Plus blood lead analyzers with part number 82-0001 that may overheat if AA batteries are placed incorrectly. This could cause burns if the batteries are removed while hot.
Incorrect AA battery placement can cause the batteries to overheat. If removed while hot, users might burn their fingers. This is a risk during normal use but not immediate.
Users of LeadCare Plus blood lead analyzers with battery boards B or O are affected. People who test blood lead levels at home are most at risk.
Check for part number 82-0001 on the device. Affected models include LeadCare II and LeadCare Plus with battery boards B or O.
Ensure AA batteries are correctly installed to prevent overheating.
If batteries are hot, do not remove them and stop using the device immediately.
Part number 82-0001 for LeadCare Plus Blood Lead Analyzers with battery boards B or O.
Check for part number 82-0001 and battery boards B or O on the device.
The recall does not specify a fix; users should check battery placement and stop using if batteries are hot.
We’ve drafted a message you can send Magellan Diagnostics to request your refund or repair — edit it as you like.
Subject: Recall Z-1296-2018 — Magellan Diagnostics Magellan Diagnostics Hello, I own a Magellan Diagnostics that is covered by recall Z-1296-2018 from Magellan Diagnostics. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
