Reported Feb 28, 2024 · Ongoing
Baxter Exactamix Pro 1200, REF EXM12DY
Baxter Healthcare Corporation
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
Baxter Exactamix Pro 1200REF EXM12DY
- Lot codes and dates
- UDI/DI 05413765588150
- Serial Numbers
PLD2314002PLD2328001PLD2328004PLD2328042PLD2314006PLD2328002PLD2328005LD2339005
- Amount recalled
- 8 devices
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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