FDA Device recall Z-0819-2025
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port
- FDA Device
- Class II
- completed
- Published 2025-01-15
On 2025-01-15 the FDA classified a Class II recall of AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port by Applied Medical Technology, citing 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 devi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0819-2025 |
| Classification | Class II |
| Status | completed |
| Initiated | 2024-11-26 |
| Published | 2025-01-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Applied Medical Technology |
| Distribution | CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA |
Product
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Reason
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.
Identifiers
| code_info | Lot Code: Model No: E6-1222 UDI-DI: (01)00842071107086(17)270401(10)240424-628 Lot number: 240424-628 Exp. Date: 2027-04-01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0819-2025%22
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