CORFLO Safety PEG Kit Recall Issued by Avanos Medical
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Avanos Medical, Inc. is recalling 43 CORFLO Safety PEG Kits with ENFit Connector due to inclusion of lidocaine hydrochloride injection subject to a supplier quality recall.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 28, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Which Products Are Affected
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312 UDI-DI: 10350770007523 Lot Numbers: 30365232, 30367019, 30380107 Quantity: 43 kits Recall Number: Z-2339-2026 Distribution: US Nationwide distribution.
What You Should Do
No specific consumer action steps are provided in the recall notice.
Why This Matters
This is an ongoing Class II recall affecting devices distributed across the United States.
Source
FDA recall Z-2339-2026, Avanos Medical, Inc., Alpharetta, GA.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (696 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 28, 2026.
Frequently Asked Questions
Common questions about this FDA recall.