FDA Device recall Z-0698-2021
AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102
- FDA Device
- Class III
- terminated
- Published 2020-12-30
On 2020-12-30 the FDA classified a Class III recall of AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102 by Applied Medical Technology, citing the products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0698-2021 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2020-11-10 |
| Published | 2020-12-30 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Applied Medical Technology |
| Distribution | US |
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
The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
Identifiers
| code_info | Box Lot Number 200918-103; Pouch Lot Number 200902-075 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0698-2021%22
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