FDA recall, , Moderate risk
Avanos Medical CORFLO and MIC Safety PEG Kits
Corflo and MIC Safety PEG Kits contain lidocaine hydrochloride injection that was recalled for quality issues.
What happened
Avanos Medical, Inc., of Alpharetta, Georgia, began a recall on April 30, 2026, of Corflo and MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) Kits because they included lidocaine hydrochloride injection that was recalled by a supplier for quality issues. The recall was added to the FDA's Enforcement Report and classified on June 5, 2026, with nationwide distribution in the United States.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
Match your product and all the details in one listed combination.
A UDI-DI is the device identifier printed with the barcode on the device label.
CORFLO* Safety PEG Kit with ENFit¿ Connector
- UDI-DI
- 10350770007578
- 30365230
- 30367013
- 30373825
- Model/Catalog number
- 50-4320
- UDI-DI
- 10350770007516
- 30365231
- 30371022
- 30373824
- 30378385
- 30383807
- 30385321
- Model/Catalog number
- 50-5320
- UDI-DI
- 10350770007523
- 30365232
- 30367019
- 30380107
- Model/Catalog number
- 50-6312
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr Push OTW
- UDI-DI
- 10350770007790
- 30370715
- 30371329
- 30375466
- Model/Catalog number
- 7170-24
CORFLO Safety PEG Kit
- UDI-DI
- 10350770007554
- 30365227
- 30368642
- 30374529
- 30376099
- 30380696
- 30387248
- Model/Catalog number
- 30-5320
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr Push OTW
- UDI-DI
- 10350770007820
- 30371324
- 30374833
- 30384889
- 80403350
- Model/Catalog number
- 8170-20
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL
- UDI-DI
- 10350770007806
- 30371316
- 30377829
- 80403341
- Model/Catalog number
- 7180-24
CORFLO* Safety PEG Kit
- UDI-DI
- 10350770007547
- 30365228
- Model/Catalog number
- 30-6312
- UDI-DI
- 10350770007561
- 30365229
- 30376100
- Model/Catalog number
- 30-6316
- UDI-DI
- 10350770007585
- 30365226
- 30382750
- Model/Catalog number
- 30-4320
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL
- UDI-DI
- 10350770007769
- 30371312
- 30373421
- Model/Catalog number
- 7180-14
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr Push OTW
- UDI-DI
- 10350770007837
- 30371847
- 30374834
- 30378748
- 30380347
- Model/Catalog number
- 8170-24
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL
- UDI-DI
- 10350770007868
- 30371319
- 30374055
- 30383058
- 30386936
- Model/Catalog number
- 8180-24
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr Push OTW
- UDI-DI
- 10350770007813
- 30370718
- Model/Catalog number
- 8170-14
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr Push OTW
- UDI-DI
- 10350770007776
- 30370714
- 30373419
- 30374048
- 30378746
- Model/Catalog number
- 7170-20
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL
- UDI-DI
- 10350770007844
- 30371318
- 30375469
- 30383056
- Model/Catalog number
- 8180-14
CORFLO Safety PEG Kit with ENFit Connector
- UDI-DI
- 10350770007530
- 30365233
- 30367015
- 30372821
- 30378386
- Model/Catalog number
- 50-6316
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL
- UDI-DI
- 10350770007783
- 30371313
- 30371314
- 30373295
- 30373296
- 30374832
- 30378735
- 80403340
- Model/Catalog number
- 7180-20
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr Push OTW
- UDI-DI
- 10350770007752
- 30370713
- Model/Catalog number
- 7170-14
MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL
- UDI-DI
- 10350770007851
- 20133232
- 30371326
- 30378749
- 30378751
- 30379686
- 30383063
- 30383057
- 80403339
- 80403342
- Model/Catalog number
- 8180-20
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Avanos Medical, Inc.Alpharetta, Georgia
- Hazard
- Sterility problem
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98907
- Recall numbers
- Z-2333-2026 to Z-2352-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated



