FDA Device recall Z-2131-2012
Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit
- FDA Device
- Class II
- terminated
- Published 2012-08-08
On 2012-08-08 the FDA classified a Class II recall of Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit by Icu Medical, citing the firm initiated the recall due to a molding defect in a high pressure stopcock where a small percentage of the side ports could become totally occluded.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2131-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-17 |
| Published | 2012-08-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Icu Medical |
| Distribution | US |
Product
Flush Kit w 3 Way Off Stopcock Product Usage: Flush Kit
Reason
The firm initiated the recall due to a molding defect in a high pressure stopcock where a small percentage of the side ports could become totally occluded.
Identifiers
| code_info | Part Number AG8137 510(k) K052865 Lot number 2466161 |
|---|
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-2131-2012%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.