FDA Device recall Z-2894-2016
Zyno Medical Administration Set, Sterile
- FDA Device
- Class II
- terminated
- Published 2016-10-05
On 2016-10-05 the FDA classified a Class II recall of Zyno Medical Administration Set, Sterile by Zyno Medical, citing administration Set potential filter leaking.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2894-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-29 |
| Published | 2016-10-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zyno Medical |
| Distribution | US |
Product
Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80072-F Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a needle or a catheter inserted into a vein.
Reason
Administration Set potential filter leaking
Identifiers
| code_info | Lot Code: 14015257 14016574 14026116 14055563 14056558 14056578 14056564 14097009 14105233 14105981 14106122…Lot Code: 14015257 14016574 14026116 14055563 14056558 14056578 14056564 14097009 14105233 14105981 14106122 14115694 14116060 14116061 15035164 15036531 15036532 15066217 15086619 15096764 15096765 15096843 15105499 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2894-2016%22
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