FDA Device recall Z-2672-2014
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005
- FDA Device
- Class II
- terminated
- Published 2014-10-01
On 2014-10-01 the FDA classified a Class II recall of EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005 by Vidacare, citing the voluntary recall is due to the needle set not meeting its specifications.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2672-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-31 |
| Published | 2014-10-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Vidacare |
| Distribution | US |
Product
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Reason
The voluntary recall is due to the needle set not meeting its specifications.
Identifiers
| code_info | Part number 9079-VC-005; lot code 3606455 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2672-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.