Drug & Device Safety Atlas

FDA recall record · openFDA

Applied Medical Technology Inc

11 FDA recalls on record (2024–2025) — 11 device. 11 still ongoing.

0
Class I (most serious)
11
Class II
0
Class III
11
ongoing

How to read this. A recall count is not a quality verdict — large manufacturers recall more simply by volume, and a voluntary recall is the safety system working as intended. The signal to weight is the Class I count (the FDA's most-serious tier — reasonable probability of serious harm or death) and whether recalls are still ongoing. Most recalls are Class II/III. "Ongoing" reflects openFDA's last-published status — device recalls often stay marked ongoing long after they're resolved in practice; confirm current status at the FDA.

Most common reasons

The nasal feeding tube may be occluded 5
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forc 4
Devices were labelled with the incorrect guidewire labelling. 1
The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFi 1

Recalls

RECORDED — these are the FDA's published recall enforcement records (openFDA). Recalls are listed under the exact firm name as filed; a large manufacturer may also file under name variants, so this may not be the company's complete cross-variant record — confirm at the FDA recall database. This page informs and routes; it is not medical advice or a verdict on the company.

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