Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit… — Class II medical device recall Z-2344-2026
Ongoing recall by Avanos Medical, Inc., reported 2026-06-17, distributed nationwide. Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into ste
| Recall number | Z-2344-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Avanos Medical, Inc., Alpharetta, GA, United States |
| Recall initiated | 2026-04-30 |
| Classified | 2026-06-05 |
| Reported by FDA | 2026-06-17 |
| Distributed | Nationwide (US) |
| Quantity | 208 kits |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10350770007769 |
| Lot numbers | 30371312, 30373421 |
| Model numbers | 7180-14 |
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14
Reason for recall
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2344-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.