Reported May 27, 2020 · Terminated
Prismaflex Control Unit
Baxter Healthcare Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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?
- Prismaflex Control Unit
- Lot codes and dates
- Product Code114870
- Lot Number
PA18198PA18199PA18238PA22556PA22558
- Amount recalled
- 5 devices US territories
Where it was sold
Why it was recalled
Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.
This product could cause temporary or reversible health problems — stop using it.
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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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