AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in patients who cannot absorb adequate nutrition through the stomach.

Recall Insight

This FDA Devices action (record #Z-1497-2016) was formally reported on April 20, 2016, with the manufacturer initiating the action on January 26, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Applied Medical Technology Inc is listed as the recalling firm, operating out of Brecksville, OH. Federal records indicate 20 units units are affected.

The documented reason for this recall is: The firm received complaints that the product is shorter in length than indicated on the label. Distribution data in the federal record shows the product reached: Distributed in the states of AZ, CA, DE, IN, MI, NM, PA & VA.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.