FDA Device recall Z-2251-2013
Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer IV fluids
- FDA Device
- Class II
- terminated
- Published 2013-09-25
On 2013-09-25 the FDA classified a Class II recall of Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer IV fluids by Churchill Medical Systems, citing microbore tubing disconnecting from male luers on the extension sets.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2251-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-08-12 |
| Published | 2013-09-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Churchill Medical Systems |
| Distribution | US |
Product
Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer IV fluids.
Reason
Microbore tubing disconnecting from male luers on the extension sets.
Identifiers
| code_info | 1203117, 1206030, 1212111, 1304133, 130516 |
|---|
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-2251-2013%22
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