AMT Mini Enteral Extension Set — Class II medical device recall Z-0819-2025
Completed recall by Applied Medical Technology Inc, reported 2025-01-15, distributed in CA, CT, FL, GA, IL, MA, MD, MO…. The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connect
| Recall number | Z-0819-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Applied Medical Technology Inc, Brecksville, OH, United States |
| Recall initiated | 2024-11-26 |
| Classified | 2025-01-07 |
| Reported by FDA | 2025-01-15 |
| Distributed | CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA |
| Quantity | 100 |
| UPC / GTIN / UDI-DI | 00842071107086 |
| Lot numbers | 240424-628 |
| Model numbers | E6-1222 |
| Expiration dates | 2027-04-01 |
Product
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Reason for recall
The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.
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-0819-2025. 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.