FDA Device recall Z-1421-2018
Manometer, 550 ml three-Way Stopcock
- FDA Device
- Class II
- terminated
- Published 2018-04-25
On 2018-04-25 the FDA classified a Class II recall of Manometer, 550 ml three-Way Stopcock by Carefusion 2200, citing the integrity of the sterile packaging is potentially compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1421-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-23 |
| Published | 2018-04-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Carefusion 2200 |
| Distribution | US |
Product
Manometer, 550 ml three-Way Stopcock; STERILE;
Reason
The integrity of the sterile packaging is potentially compromised.
Identifiers
| code_info | Product Code: 4330 Lot Code: 0000837810; 0000840335; 0000842213; 0000848531; 0000851181; 0000853962 |
|---|
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-1421-2018%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.