Drug recall
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
FDA recall event 85260 · Class II · Avanos Medical, Inc.
Key facts
| Event ID | 85260 |
|---|---|
| Recall numbers | Z-1822-2020 |
| Recalling firm | Avanos Medical, Inc. |
| Product type | Devices |
| Products | CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted. |
| Initiation date | Mar 16, 2020 |
| Report date | May 6, 2020 |
| Termination date | Aug 31, 2023 |
| 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: