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Applied Medical Technology Inc recalls AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Recalled July 10, 2024 · FDA recall Z-2238-2024 · Applied Medical Technology
Hazard
Devices were labelled with the incorrect guidewire labelling. · FDA Class II
Units
74 units
Sold at
US Nationwide distribution in the states of GA, IL, IN, LA, NC, NE, SC, TN, TX, UT, VA, WA, & WV.
Description
Devices were labelled with the incorrect guidewire labelling.
Product
AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Manufacturer(s)
Applied Medical Technology Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →