Applied Medical Technology Inc: Device Recall
Recall #Z-2238-2024 · 05/14/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2238-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Applied Medical Technology Inc
- Status
- Ongoing
- Date Initiated
- 05/14/2024
- Location
- Brecksville, OH, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 74 units
Reason for Recall
Devices were labelled with the incorrect guidewire labelling.
Product Description
AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Distribution Pattern
US Nationwide distribution in the states of GA, IL, IN, LA, NC, NE, SC, TN, TX, UT, VA, WA, & WV.
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.