Diagnostic Imaging Tray — Class II medical device recall Z-0944-2015
Terminated recall by Centurion Medical Products Corporation, reported 2015-01-14, distributed nationwide. According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer rep
| Recall number | Z-0944-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2014-10-23 |
| Classified | 2015-01-08 |
| Reported by FDA | 2015-01-14 |
| Terminated | 2015-06-08 |
| Distributed | Nationwide (US) |
| Quantity | 760 kits |
| Reason classes | specification failure |
| Lot numbers | 2014061250, 2015-11 |
Product
Diagnostic Imaging Tray (General Surgery convenience kit)
Reason for recall
According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
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-0944-2015. 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.