FDA Device recall Z-0084-2015
Baxter 2B8011 Empty INTRA VIA Container with PVC Ports, Sterile fluid path, 150 ml, Admixture Products and Accessories
- FDA Device
- Class I
- terminated
- Published 2014-11-12
On 2014-11-12 the FDA classified a Class I recall of Baxter 2B8011 Empty INTRA VIA Container with PVC Ports, Sterile fluid path, 150 ml, Admixture Products and Accessories by Baxter Healthcare, citing particulate matter found inside the fluid path.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0084-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-09-16 |
| Published | 2014-11-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter 2B8011 Empty INTRA VIA Container with PVC Ports, Sterile fluid path, 150 ml, Admixture Products and Accessories. The lntraVia Empty Plastic Container is intended for use in the preparation and administration of drug admixtures.
Reason
Particulate matter found inside the fluid path.
Identifiers
| code_info | Product code: 2B8011 Lot Number: UR13D15112 |
|---|
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-0084-2015%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.