Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AMT Initial Placement Dilator Set. Used to place gastrostomy devices. Recalled by Applied Medical Technology Inc Due to Devices were labelled with the incorrect guidewire labelling.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Applied Medical Technology Inc directly.
Affected Products
AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Quantity: 74 units
Why Was This Recalled?
Devices were labelled with the incorrect guidewire labelling.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Applied Medical Technology Inc
Applied Medical Technology Inc has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report