Class II — Avanos Medical, Inc.
| Recalling firm | Avanos Medical, Inc. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Devices had cracked or detached from the feeding tube body |
| Product | AVANOS MIC-KEY SF Gastrostomy Feeding Tube |
| Quantity | 284 units |
| Distribution | US states: OK IL WI PA TX IL PA NJ OK LA OUS: Belgium |
| Initiated | 2020-07-29 |
| Classified | 2020-09-14 |
| Terminated | 2023-01-31 |
| Recall number | Z-2969-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Avanos Medical, Inc. (Z-2969-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86244/
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