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FDAFDA · Food and drugs·Recall number Z-0556-2014

McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).

Published January 1, 2014 · Recall initiated: October 15, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

When merging two patient records into one patient record using McKesson Radiology 12.0, the resulting patient record is missing the Contrast Allergy information for the second patient record.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Mckesson Information Solutions LLC
Distributor
MO, NY, TN, WV and France.
Lot
MR 12.0
Risk classification
Class II
Area (FDA)
device
Country
United States

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