FDA Device recall Z-2433-2019
Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems
- FDA Device
- Class II
- terminated
- Published 2019-09-11
On 2019-09-11 the FDA classified a Class II recall of Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems by Getinge Us Sales, citing reversed expiration and manufacturing date on the label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2433-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-22 |
| Published | 2019-09-11 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Getinge Us Sales |
| Distribution | US |
Product
Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
Reason
Reversed expiration and manufacturing date on the label
Identifiers
| code_info | Lot # 1810, 1811 Part Number: 6677845 for 12 pcs, 6673717 for 1 pcs UDI Code: 17325710001988 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2433-2019%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.