GEM FLOW COUPLER Monitor, PN 5156-00000-011
FDA Recall Z-2208-2023 · Posted 2023-07-20
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Recalling FirmBaxter Healthcare Corporation
Recall StatusOpen, Classified
Product CodeDPW
Date Initiated2023-06-19
Product Quantity122 units
Reason for Recall
An issue was identified where the LCD monitor display may not indicate the correct active channel. The issue occurs when the monitor is turned on using battery power, and channel B was selected as the last active channel prior to powering down.
Firm Action
Synovis Micro Companies Alliance (MCA), Inc., a subsidiary of Baxter International Inc.,
is issuing an Urgent Medical Device Correction to its consignees on 06/19/2023 by USPS First Class Mail. The notice explained the problem with the device, risk, and provided the following method to circumvent the problem:
"The affected flow coupler monitors may continue to be used. To avoid encountering
this issue, please use the monitor while connected to an AC power supply whenever
possible.
However, if using battery power, Baxter advises users to select channel A prior to
shutting down the monitor. Upon powering the monitor back up, please check to
ensure that the channel illuminated via the hardware button matches the LCD
screen channel display. If a mismatch occurs, touch the channel display on the LCD
screen or press the hardware button for channel B to resolve the issue.
For general questions regarding this communication, please contact Synovis MCA at
800-510-3318 or 205-941-0111, between the hours of 8:00 am and 5:00 pm Central
Time, Monday through Friday."
Root Cause
Under Investigation by firm
Distribution Pattern
US
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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