CORFLO Percutaneous Endoscopic Gastrostomy — Class II medical device recall Z-1822-2020
Terminated recall by Avanos Medical, Inc., reported 2020-05-06, distributed nationwide. The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure
| Recall number | Z-1822-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Avanos Medical, Inc., Alpharetta, GA, United States |
| Recall initiated | 2020-03-16 |
| Classified | 2020-04-29 |
| Reported by FDA | 2020-05-06 |
| Terminated | 2023-08-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BE, CA, DE, FR, GB, IE, IT, NL, RO |
| Quantity | 1,766 |
| Lot numbers | 0002994170, 0002994171, 0002994174, 0002997217, 0002997221, 0020003029, 0020003356, 0020006332, 0020008354, 0020008544, 0020008547, 0020008666, 0203214820, 0203214901, 0203214902, 0203214903, 0203214905, 0203239802, 0203239803, 0203239804, 0203241062, 0203241063, 0203241064, 0203245676, 0203245678, 0203248168, 0203251785, 0203251786, 0203251843, 0203251844, 0203261078, 0203261079, 20011367, 20011369, 20012261, 2001368 |
Product
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
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.
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-1822-2020. 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.