Fresh Recalls

FDAClass II · Medical device · Recall Z-2339-2026 · Recalled June 17, 2026

Product Name recall — Avanos Medical, Inc.

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Product Name
Company / brand
Avanos Medical
Lot / serial / date codes
UDI-DI 10350770007523, Lot Numbers 30365232, 30367019, 30380107
Distribution
US Nationwide distribution.
Agency product description and boundaries

Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Product Name recall status

3. Open the official notice or contact

Official recall ID
Z-2339-2026
Brand
All Avanos Medical recalls
Classification
Class II
Units affected
43 kits
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Alpharetta, GA, United States
Firm address
5405 Windward Pkwy, N/A, 30004-4667

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI 10350770007523, Lot Numbers 30365232, 30367019, 30380107
Distribution
US Nationwide distribution.
Firm notified the public via
N/A
FDA event ID
98907
Recall initiated
April 30, 2026
FDA classified
June 5, 2026
FDA report date
June 17, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 15, 2026 at 6:00 PM UTC.

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