Applied Medical Technology Inc recalls Applied Medical Technology

The nasal feeding tube may be occluded

Applied Medical Technology, Inc. issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 10/06/2025 via certified mail. The notice explained the issue, potential risk to health, and requested the consignee quarantine the affected product, complete and return the acknowledgement, and contact Applied Medical Technology, Inc. either by telephone at 440-717-4000 or via email at cs@appliedmedical.net to arrange for the return of the affected product. Those who further distributed the product were directed to notify those to whom the product was transferred of this recall. For questions or concerns, contact: Customer Service, 440-717-4000 (tel), 440-717-4200 (fax), cs@appliedmedical.net (email). Hours of operation 8:30 A - 5:00 P, Eastern time

• FDA enforcement recordOfficial FDA database entry for Z-0497-2026
• FDA 510(k) clearance · K202539The device's official FDA premarket clearance record
• FDA device classification · KNTOfficial FDA classification for this device type
• CFR regulation · 21 CFR 876.5980The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Applied Medical Technology IncSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.