Avanos CORFLO Safety PEG Kit with ENFit Connector Recall: Lidocaine Quality Issues
Avanos Medical recalls CORFLO Safety PEG Kit with ENFit Connector (model 50-4320) due to lidocaine hydrochloride injection quality issues in sterile kits. Affected units include specific lot numbers and UDI-DI codes.
Lower-risk recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Contact the company
What happened, in plain English
Avanos Medical is recalling its CORFLO Safety PEG Kit with ENFit Connector (model 50-4320) because lidocaine hydrochloride injections were included in sterile kits during manufacturing. This could lead to contamination risks if the kit is used for medical procedures. Read more at govinfonow.com/recall/49262-avanos-corflo-safety-peg-kit-with-enfit-connector-recall-lidocaine.
Source Summary by GovInfoNow · govinfonow.com/recall/49262-avanos-corflo-safety-peg-kit-with-enfit-connector-recall-lidocaine · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2337-2026
Cite this page
“Avanos CORFLO Safety PEG Kit with ENFit Connector Recall: Lidocaine Quality Issues.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49262-avanos-corflo-safety-peg-kit-with-enfit-connector-recall-lidocaine. Based on FDA recall #Z-2337-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2337-2026%22&limit=1).
Why it’s dangerous
Lidocaine hydrochloride injections were included in sterile kits during manufacturing, which could lead to contamination. This poses a risk of improper medication delivery if the kit is used for medical procedures.
Who’s affected
Healthcare professionals using the CORFLO Safety PEG Kit with ENFit Connector for medical procedures are most at risk. Patients receiving injections through this kit could be affected if the lidocaine is contaminated.
How to tell if you have this one
Check for the model number 50-4320 on the kit. Look for UDI-DI code 10350770007578 and lot numbers 30365230, 30367013, or 30373825.
- Brand
Avanos Medical- Category
Medical device
All 20 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-2333-2026 | Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320; UDI-DI 10350770007585, Lot Numbers 30365226 and 30382750 | 231 kits |
| Z-2334-2026 | Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 30-5320; UDI-DI 10350770007554, Lot Numbers 30365227, 30368642, 30374529, 30376099, 30380696, and 30387248 | 61 kits |
| Z-2335-2026 | Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312; Lot Code: Model No 30-6312, UDI-DI 10350770007547, Lot Number 30365228 | 31 kits |
| Z-2336-2026 | Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316; Lot Code: Model No 30-6316, UDI-DI 10350770007561, Lot Numbers 30365229 and 30376100 | 41 kits |
| Z-2337-2026 | Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320; UDI-DI 10350770007578, Lot Numbers 30365230, 30367013, 30373825 | 49 kits |
| Z-2338-2026 | Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320; UDI-DI 10350770007516, Lot Numbers 30365231, 30371022, 30373824, 30378385, 30383807, 30385321 | 72 kits |
| Z-2339-2026 | Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312; UDI-DI 10350770007523, Lot Numbers 30365232, 30367019, 30380107 | 43 kits |
| Z-2340-2026 | Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-6316 Product Description: Feeding Tube Kit Component: No; UDI-DI 10350770007530, Lot Numbers 30365233, 30367015, 30372821, 30378386 | 54 kits |
| Z-2341-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit; UDI-DI 10350770007752, Lot Number 30370713 | 22 kits |
| Z-2342-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUSH OTW Model/Catalog Number: 7170-20 Product Description: Feeding Tube Kit Component: No; Lot Code: Model No 7170-20, UDI-DI 10350770007776, Lot Numbers 30370714, 30373419, 30374048, 30378746 | 901 kits |
| Z-2343-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: Feeding Tube Kit Component: No; UDI-DI: 10350770007790, Lot Numbers 30370715, 30371329, 30375466 | 132 kits |
| Z-2344-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14; UDI-DI 10350770007769, Lot Numbers 30371312 and 30373421 | 208 kits |
| Z-2345-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20; UDI-DI 10350770007783, Lot Numbers 30371313, 30371314, 30373295, 30373296, 30374832, 30378735, 80403340 | 3,184 kits |
| Z-2346-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24; UDI-DI 10350770007806, Lot Numbers 30371316, 30377829, 80403341 | 1,006 kits |
| Z-2347-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No; UDI-DI 10350770007813, Lot Number 30370718 | 53 kits |
| Z-2348-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PUSH OTW Model/Catalog Number: 8170-20; UDI-DI 10350770007820, Lot Numbers 30371324, 30374833, 30384889, 80403350 | 1,615 kits |
| Z-2349-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24; UDI-DI 10350770007837, Lot Numbers 30371847, 30374834, 30378748, 30380347 | 234 kits |
| Z-2350-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14; UDI-DI 10350770007844, Lot Numbers 30371318, 30375469, 30383056 | 218 kits |
| Z-2351-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20; Lot Code: Model No 8180-20, UDI-DI 10350770007851, Lot Numbers 20133232, 30371326, 30378749, 30378751, 30379686, 30383063, 30383057, 80403339, 80403342 | 6,005 kits |
| Z-2352-2026 | Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24; UDI-DI 10350770007868, Lot Numbers 30371319, 30374055, 30383058, 30386936 | 1,205 kits |
What to do — step by step
Check Kit Details
Verify the model number (50-4320), UDI-DI code (10350770007578), and lot numbers (30365230, 30367013, 30373825) to confirm if your kit is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 48 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2337-2026 (April 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2337-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.