Bard Medical recalls Arctic Sun 5000 temperature management systems due to wiring issues that may cause overheating and component failure. Affected models include 5000-00-00 to 5000-01-08 with all serial numbers.
An improper wiring connection on the chiller assembly may result in overheating of the connection and potential failure of certain components in the system.
Bard Medical is recalling its Arctic Sun 5000 temperature management system because improper wiring could cause overheating and component failure. This poses a risk of system malfunction during patient temperature monitoring.
Improper wiring in the chiller assembly may cause overheating, which can lead to component failure. This could disrupt temperature monitoring and potentially cause unsafe temperature conditions for patients.
Adults and pediatric patients using the Arctic Sun 5000 system for temperature monitoring are affected. Patients with medical conditions requiring precise temperature control are at higher risk.
Check for the model numbers 5000-00-00 through 5000-01-08 or all serial numbers on the device. The product is a non-invasive thermal regulating system used for patient temperature monitoring.
Inspect the chiller assembly for proper wiring connections to ensure they are secure and not overheating.
All models with product codes 5000-00-00 to 5000-01-08 and all serial numbers are affected.
The recall record does not specify a fix or remedy for this issue.
Check the product code on your device; affected models include 5000-00-00 through 5000-01-08 with all serial numbers.
We’ve drafted a message you can send Bard Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2536-2018 — Bard Medical Bard Medical Hello, I own a Bard Medical that is covered by recall Z-2536-2018 from Bard Medical. 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.
