APPLIED MEDICAL TECHNOLOGY, INC.
8 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (8)
Registered facilities (1)
- APPLIED MEDICAL TECHNOLOGY, INC. FEI 1526012 · OH
Recalls & enforcement
- Class IICompleted2025-10-06The nasal feeding tube may be occluded
- Class IICompleted2025-08-12The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Class IICompleted2024-11-26The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.
- Class IICompleted2024-05-14Devices were labelled with the incorrect guidewire labelling.
- Class IIITerminated2020-11-10The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
- Class IIITerminated2017-01-19Expired expiration dates are listed on the pouches.
- Class IITerminated2016-02-17The firm received a complaint of an open pouch which breaches the sterilization validation.
- Class IITerminated2016-01-26The firm received complaints that the product is shorter in length than indicated on the label.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “APPLIED MEDICAL TECHNOLOGY, INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-1526012-applied-medical-technology-inc/
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