Baxter Exactamix Pro 1200, REF EXM12DY
FDA Recall Z-1001-2024 · Posted 2024-02-16
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Recalling FirmBaxter Healthcare Corporation
Recall StatusOpen, Classified
Product CodeLHI
Date Initiated2023-12-22
Product Quantity8 devices
Reason for Recall
An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant ingredient delivery of the requested overfill volume.
Firm Action
Baxter issued an Urgent Medical Device Correction notice to its consignees on 12/22/2023 via USPS First Class mail. The notice explained the issue with the device, potential risks, and requested the following actions be taken for the safe operation until a software upgrade is released:
"1. Operators may continue to use the ExactaMix Pro compounders, but when the
system prompts the operator that ingredients are depleted, operators should choose
to Swap Container or Use a Different Container and not utilize the Use Some
Overfill feature until further notice by Baxter. For more information on alternatives
to using overfill, refer to the information on Replacing a Source Container on pages
82-83 in the ExactaMix Pro 2400 Operator Manual and pages 83-84 in the
ExactaMix Pro 1200 Operator Manual.
2. If the Use Some Overfill feature is inadvertently used, operators must ensure that:
o The Use Some Overfill feature is used only ONCE when an ingredient is
depleted.
o When prompted to enter the volume of overfill to use, enter LESS THAN the
volume left to run stated in the Swap Container window.
o On the MixCheck report, verify that all ingredient deliveries that used overfill
volume delivered the expected ingredient volume and that the final total
volume for the bag aligns with the expected volume.
o If you observe redundant ingredient delivery using the overfill volume per
the MixCheck report, discard the bag.
3. Always review the final MixCheck report as described in the ExactaMix Pro
Operator Manual. Please review the information on this feature on pages 167-171
in the ExactaMix Pro 2400 Operator Manual and pages 164-168 in the ExactaMix
Pro 1200 Operator Manual.
4. A Baxter representative will contact your facility when the software upgrade becomes available. Please note you will be receiving this upgrade from Baxter at no charge."
If the affected product was distributed to other facilities or departments within your institution, please forward a copy of
Root Cause
Device Design
Distribution Pattern
US: AL, AZ, CA, FL, GA, IA, KY, MD, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OR, SD, TX, WA, WI,
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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