EZ-IO 45mm — Class II medical device recall Z-2672-2014
Terminated recall by Vidacare Corporation, reported 2014-10-01, distributed nationwide. The voluntary recall is due to the needle set not meeting its specifications.
| Recall number | Z-2672-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vidacare Corporation, San Antonio, TX, United States |
| Recall initiated | 2014-03-31 |
| Classified | 2014-09-22 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2015-01-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 172 |
| Lot numbers | 3606455 |
| Model numbers | 9079-VC-005 |
Product
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Reason for recall
The voluntary recall is due to the needle set not meeting its specifications.
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-2672-2014. 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.