SECURE — Class II medical device recall Z-3240-2017
Terminated recall by The Metrix Company, reported 2017-10-11, distributed in AZ, FL, IL, MA. The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are corr
| Recall number | Z-3240-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | The Metrix Company, Dubuque, IA, United States |
| Recall initiated | 2017-09-13 |
| Classified | 2017-09-29 |
| Reported by FDA | 2017-10-11 |
| Terminated | 2018-05-25 |
| Distributed | AZ, FL, IL, MA |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 50812496011850 |
| Lot numbers | 28990, 29093, 29135, 29244 |
| Model numbers | 58719 |
Product
SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,
Reason for recall
The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as ordered and as labeled on the inner and outer boxes.
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-3240-2017. 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.