CORFLO Safety PEG Kit Recall Issued
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Avanos Medical is recalling 54 CORFLO Safety PEG Kits with ENFit Connector nationwide after including 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 Avanos Medical, Inc. initiated a voluntary recall of certain feeding tube kits after lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, was included in the sterile kits and sets.
Which Products Are Affected The affected product is the CORFLO Safety PEG Kit with ENFit Connector, model/catalog number 50-6316. Additional details include UDI-DI 10350770007530 and lot numbers 30365233, 30367015, 30372821, 30378386. A total of 54 kits were distributed via US Nationwide distribution.
What You Should Do The recall notice does not specify consumer actions. Affected parties should contact the recalling firm for further guidance.
Why This Matters The inclusion of recalled components in sterile medical device kits may affect product integrity for patients using feeding tubes.
Source FDA recall number Z-2340-2026, event ID 98907.
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 (903 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.