RegWardenFDA facility compliance records
Recall

Class III — Applied Medical Technology Inc

Recalling firmAPPLIED MEDICAL TECHNOLOGY, INC.
Registered facilityAPPLIED MEDICAL TECHNOLOGY, INC. (the firm's only registered facility)
ClassificationClass III
StatusTerminated
ReasonThe products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
ProductAMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI (01)00842071109066(17)230901(10)200918-103, Pouch PN ETRN102, Pouch UDI (01)00842071108007(17)230901(10)200902-075
QuantityN/A
DistributionUS Nationwide distribution in the states of CA, GA, IL, MA, MO, PA, TX, VA. No foreign distribution.
Initiated2020-11-10
Classified2020-12-23
Terminated2021-09-03
Recall numberZ-0698-2021
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class III recall — Applied Medical Technology Inc (Z-0698-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86828/

Not open yet

Alerts for APPLIED MEDICAL TECHNOLOGY, INC.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.