Drug recall
Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
FDA recall event 98907 · Class II · Avanos Medical, Inc.
Key facts
| Event ID | 98907 |
|---|---|
| Recall numbers | Z-2333-2026, Z-2334-2026, Z-2335-2026, Z-2336-2026, Z-2337-2026, Z-2338-2026, Z-2339-2026, Z-2340-2026, Z-2341-2026, Z-2342-2026, Z-2343-2026, Z-2344-2026 and 8 more |
| Recalling firm | Avanos Medical, Inc. |
| Product type | Devices |
| Products | Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320, Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320, Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312, Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316, Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320 and 15 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets. |
| Initiation date | Apr 30, 2026 |
| Report date | Jun 17, 2026 |
| City | Alpharetta |
| State | GA |
| Country | United States |
| FEI number | 3011270181 |
At a glance
- 10–99 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: