Drug recall
Avanos Cortrak 2 Enteral Access System (EAS)
FDA recall event 89997 · Class I · Avanos Medical, Inc.
Key facts
| Event ID | 89997 |
|---|---|
| Recall numbers | Z-1032-2022 |
| Recalling firm | Avanos Medical, Inc. |
| Product type | Devices |
| Products | Avanos Cortrak 2 Enteral Access System (EAS) |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol. |
| Initiation date | Mar 21, 2022 |
| Report date | May 25, 2022 |
| Termination date | Sep 9, 2024 |
| City | Alpharetta |
| State | GA |
| Country | United States |
| FEI number | 3011270181 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: