General Electric Medical Systems Information Technology MAC-LAB (Classic) systems Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MAC-LAB (Classic) systems
Brand
General Electric Medical Systems Information Technology
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
The affected systems have serial numbers with XC and 4A as 3rd and 4th characters in the serial number
General Electric Medical Systems Information Technology is recalling MAC-LAB (Classic) systems due to There is an incorrect jumper set-up on a motherboard of the devices that could eventually cause a polyfuse to overheat resulting in smoke.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is an incorrect jumper set-up on a motherboard of the devices that could eventually cause a polyfuse to overheat resulting in smoke.
Recommended Action
Per FDA guidance
A letter was sent to the consignees on April 14, 2003 and requested that the consignees correct the device or contact the firm to have them perform the correction.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026