Sunquest Application Interfacing Outbound Phlebotomy Point of Care… — Class II medical device recall Z-0251-2013
Terminated recall by Sunquest Information Systems, Inc., reported 2012-11-14, distributed nationwide. The recall was initiated because Sunquest Information System has confirmed reports of an Outbound Phlebotomy P
| Recall number | Z-0251-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sunquest Information Systems, Inc., Tucson, AZ, United States |
| Recall initiated | 2009-11-19 |
| Classified | 2012-11-06 |
| Reported by FDA | 2012-11-14 |
| Terminated | 2012-11-06 |
| Distributed | Nationwide (US) |
| Quantity | 9 units |
Product
Sunquest Application Interfacing Outbound Phlebotomy Point of Care Interface, v3.0.0_07222004 and later.
Reason for recall
The recall was initiated because Sunquest Information System has confirmed reports of an Outbound Phlebotomy Point of Care (POC) interface is combining patient orders inappropriately.
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-0251-2013. 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.