Applied Medical Technology Inc: Device Recall
Recall #Z-0819-2025 · 11/26/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0819-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Applied Medical Technology Inc
- Status
- Ongoing
- Date Initiated
- 11/26/2024
- Location
- Brecksville, OH, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 100
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.
Product Description
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Distribution Pattern
US Distribution to states of: CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA
Other Recalls by Applied Medical Technology Inc
- Class II: Risk 10/06/2025
- Class II: Risk 10/06/2025
- Class II: Risk 10/06/2025
- Class II: Risk 10/06/2025
- Class II: Risk 10/06/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.