Getinge MCC Flow i Disposable CO2 absorber — Class II medical device recall Z-2433-2019
Terminated recall by GETINGE US SALES LLC, reported 2019-09-11, distributed nationwide. Reversed expiration and manufacturing date on the label
| Recall number | Z-2433-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GETINGE US SALES LLC, WAYNE, NJ, United States |
| Recall initiated | 2019-07-22 |
| Classified | 2019-08-30 |
| Reported by FDA | 2019-09-11 |
| Terminated | 2020-05-26 |
| Distributed | Nationwide (US) |
| Quantity | 1,444 boxes |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 17325710001988 |
| Lot numbers | 1810, 1811 |
| Model numbers | 6673717, 6677845 |
Product
Getinge MCC Flow i Disposable CO2 absorber, used in anesthesia systems.
Reason for recall
Reversed expiration and manufacturing date on the label
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2433-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.