McKesson Radiology 12 — Class II medical device recall Z-0556-2014
Terminated recall by Mckesson Information Solutions LLC, reported 2014-01-01, distributed in MO, NY, TN, WV. When merging two patient records into one patient record using McKesson Radiology 12.0, the resulting patient
| Recall number | Z-0556-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Information Solutions LLC, Alpharetta, GA, United States |
| Recall initiated | 2013-10-15 |
| Classified | 2013-12-20 |
| Reported by FDA | 2014-01-01 |
| Terminated | 2014-06-03 |
| Distributed | MO, NY, TN, WV |
| Countries outside the US | FR |
| Quantity | 6 units |
Product
McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0556-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.