AMT Male ENFit-to-Stepped Male — Class III medical device recall Z-0698-2021
Terminated recall by Applied Medical Technology Inc, reported 2020-12-30, distributed nationwide. The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the co
| Recall number | Z-0698-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Applied Medical Technology Inc, Brecksville, OH, United States |
| Recall initiated | 2020-11-10 |
| Classified | 2020-12-23 |
| Reported by FDA | 2020-12-30 |
| Terminated | 2021-09-03 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00842071108007, 00842071109066 |
| Lot numbers | 200902-075, 200918-103 |
| Model numbers | ETRN102, TRN102 |
Product
AMT 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
Reason for recall
The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0698-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.