FDA Device recall Z-1473-2015
7" High Pressure Set with Bionector, Product Code: CMS-808 and CMS-808-1 Accessory device used to administer medical fluids
- FDA Device
- Class II
- terminated
- Published 2015-04-29
On 2015-04-29 the FDA classified a Class II recall of 7" High Pressure Set with Bionector, Product Code: CMS-808 and CMS-808-1 Accessory device used to administer medical fluids by Churchill Medical Systems, citing potential for leaking caused by insufficient bond between needleless device and female luer.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1473-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-15 |
| Published | 2015-04-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Churchill Medical Systems |
| Distribution | US |
Product
7" High Pressure Set with Bionector, Product Code: CMS-808 and CMS-808-1 Accessory device used to administer medical fluids
Reason
Potential for leaking caused by insufficient bond between needleless device and female luer.
Identifiers
| code_info | 1303184 1304184 1305112 1306088 1309061 1311057 1312168 1401125 1402017 1403050 1404052 1405018 1405106 14…1303184 1304184 1305112 1306088 1309061 1311057 1312168 1401125 1402017 1403050 1404052 1405018 1405106 1406151 1407065 1408054 1409122D 1410064D 1410155D 1410156D |
|---|
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-1473-2015%22
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