Applied Medical Technology AMT Male ENFit Adapter Recall: Incorrect Pouch Labels
Applied Medical Technology recalls AMT Male ENFit-to-Stepped Male adapters with incorrect pouch labels. Consumers should check labels to avoid using faulty products.
Lower-risk recall
The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
Contact the company
What happened, in plain English
Applied Medical Technology is recalling male ENFit-to-stepped male adapters that may have incorrect pouch labels. This could lead to confusion during medical use, but the recall does not indicate a safety hazard. Read more at govinfonow.com/recall/63950-applied-medical-technology-amt-male-enfit-adapter-recall-incorrect-pouch.
Source Summary by GovInfoNow · govinfonow.com/recall/63950-applied-medical-technology-amt-male-enfit-adapter-recall-incorrect-pouch · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0698-2021
Cite this page
“Applied Medical Technology AMT Male ENFit Adapter Recall: Incorrect Pouch Labels.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63950-applied-medical-technology-amt-male-enfit-adapter-recall-incorrect-pouch. Based on FDA recall #Z-0698-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0698-2021%22&limit=1).
Why it’s dangerous
The adapters may have incorrect pouch labels compared to the outer box. This could cause confusion during medical procedures but does not pose a direct safety risk.
Who’s affected
Patients using medical adapters with incorrect pouch labels may be affected. Healthcare providers and patients who use these adapters are most at risk.
How to tell if you have this one
Check the pouch label for the model number ETRN102 and the lot number 200902-075. The outer box should have the correct label and model number.
- Brand
Applied Medical Technology- Product
AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI- Category
Medical device
What to do — step by step
Check Pouch Label
Look for the model number ETRN102 and lot number 200902-075 on the pouch label.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 8 states.
FDA distribution: “US Nationwide distribution in the states of CA, GA, IL, MA, MO, PA, TX, VA. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Georgia, Illinois, Massachusetts, Missouri, Pennsylvania, Texas, Virginia.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using the product?
No, the recall does not require stopping use. The issue is label confusion, not a safety hazard.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0698-2021 (November 10, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0698-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.